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Grandiosity
Wikipedia
PMID 19486844 . v t e Narcissism Types Collective Egomania Flying monkeys Healthy Malignant Narcissistic personality disorder Spiritual Workplace Characteristics Betrayal Boasting Egocentrism Egotism Empathy (lack of) Envy Entitlement (exaggerated sense of) Fantasy Grandiosity Hubris Magical thinking Manipulative Narcissistic abuse Narcissistic elation Narcissistic rage and narcissistic injury Narcissistic mortification Narcissistic supply Narcissistic withdrawal Perfectionism Self-esteem Self-righteousness Shamelessness Superficial charm Superiority complex True self and false self Vanity Defences Denial Idealization and devaluation Distortion Projection Splitting Cultural phenomena Control freak Don Juanism Dorian Gray syndrome My way or the highway Selfie Related articles Codependency Counterdependency Dark triad Ego ideal "Egomania" (film) Egotheism Empire-building God complex History of narcissism Messiah complex Micromanagement Narcissism of small differences Narcissistic leadership Narcissistic parent Narcissistic Personality Inventory Narcissus (mythology) On Narcissism Sam Vaknin Self-love Self-serving bias Spoiled child The Culture of Narcissism Workplace bullying v t e Psychopathy Contexts In fiction In the workplace Characteristics Anti-social behaviour Bold Callous Diminished empathy Disinhibited Grandiose Impulsive Lack of guilt Manipulative Pathological lying Remorseless Shallow affect Superficially charming Related topics Antisocial personality disorder Conduct disorder Dark triad Flying monkeys History of psychopathy Juvenile delinquency Machiavellianism Macdonald triad Narcissism Psychopathic Personality Inventory Psychopathy Checklist Sadistic personality disorder Sexual sadism disorder Sociopathy Notable theorists Hervey M.
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Cluttering
Wikipedia
Louis, (1992) Cluttering: A Clinical Perspective, Leicester, England: Far Communications External links [ edit ] Classification D ICD - 10 : F98.6 ICD - 9-CM : 307.0 SNOMED CT : 37732008 Cluttering: Some Guidelines Overview of Cluttering International Cluttering Association page ASHA Cluttering Updated Article ISAD presentation on cluttering experience Computer Aided Assessment of Cluttering Severity v t e Emotional and behavioral disorders Emotional/behavioral ADHD Conduct disorder Oppositional defiant disorder Emotional/behavioral disorder (EBD) Separation anxiety Social functioning Selective mutism RAD DAD Tic disorders Tourette syndrome Speech disorders Stuttering Cluttering Stereotypic movement disorder Elimination disorders Enuresis Encopresis Authority control GND : 4259221-5 LCCN : sh85027260
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Urethral Stricture
Wikipedia
External links [ edit ] Classification D ICD - 10 : N35 ICD - 9-CM : 598 MeSH : D014525 DiseasesDB : 13562 External resources MedlinePlus : 001271 eMedicine : med/3075 v t e Diseases of the urinary tract Ureter Ureteritis Ureterocele Megaureter Bladder Cystitis Interstitial cystitis Hunner's ulcer Trigonitis Hemorrhagic cystitis Neurogenic bladder dysfunction Bladder sphincter dyssynergia Vesicointestinal fistula Vesicoureteral reflux Urethra Urethritis Non-gonococcal urethritis Urethral syndrome Urethral stricture Meatal stenosis Urethral caruncle Any/all Obstructive uropathy Urinary tract infection Retroperitoneal fibrosis Urolithiasis Bladder stone Kidney stone Renal colic Malakoplakia Urinary incontinence Stress Urge Overflow
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Craniopagus Parasiticus
Wikipedia
CS1 maint: uses authors parameter ( link ) External links [ edit ] Image File of craniopagus parasiticus v t e Twin conditions Zygosity Twin Monochorionic twins Twin-to-twin transfusion syndrome Twin reversed arterial perfusion Monoamniotic twins Conjoined twins Parasitic twin Craniopagus parasiticus Fetus in fetu Other Vanishing twin Chimerism Mixed twins
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Derealization
Wikipedia
Exercises with documented successes include timed intervals of hyperventilation or staring at a mirror, dot, or spiral. [13] See also [ edit ] Depersonalization Śūnyatā Ego death Temporal lobe epilepsy Post-traumatic stress disorder Dissociative disorders Existential crisis Mystical psychosis Narcissistic withdrawal Spiritual emergency Solipsism syndrome Fugue state Reality Spectacle Falling (sensation) Weltschmerz sleep deprivation References [ edit ] ^ American Psychiatric Association (2004) Diagnostic and Statistical Manual of Mental Disorders DSM-IV-TR (Text Revision).
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Neurolathyrism
Wikipedia
External links [ edit ] Classification D ICD - 10 : T62.2 ICD - 9-CM : 988.2 MeSH : D007842 DiseasesDB : 32679 SNOMED CT : 5724005 Lathyrism at the Duke University Health System 's Orthopedics program Detection of Toxic Lathyrus sativus flour in Gram Flour v t e Poisoning Toxicity Overdose History of poison Inorganic Metals Toxic metals Beryllium Cadmium Lead Mercury Nickel Silver Thallium Tin Dietary minerals Chromium Cobalt Copper Iron Manganese Zinc Metalloids Arsenic Nonmetals Sulfuric acid Selenium Chlorine Fluoride Organic Phosphorus Pesticides Aluminium phosphide Organophosphates Nitrogen Cyanide Nicotine Nitrogen dioxide poisoning CHO alcohol Ethanol Ethylene glycol Methanol Carbon monoxide Oxygen Toluene Pharmaceutical Drug overdoses Nervous Anticholinesterase Aspirin Barbiturates Benzodiazepines Cocaine Lithium Opioids Paracetamol Tricyclic antidepressants Cardiovascular Digoxin Dipyridamole Vitamin poisoning Vitamin A Vitamin D Vitamin E Megavitamin-B 6 syndrome Biological 1 Fish / seafood Ciguatera Haff disease Ichthyoallyeinotoxism Scombroid Shellfish poisoning Amnesic Diarrhetic Neurotoxic Paralytic Other vertebrates amphibian venom Batrachotoxin Bombesin Bufotenin Physalaemin birds / quail Coturnism snake venom Alpha-Bungarotoxin Ancrod Batroxobin Arthropods Arthropod bites and stings bee sting / bee venom Apamin Melittin scorpion venom Charybdotoxin spider venom Latrotoxin / Latrodectism Loxoscelism tick paralysis Plants / fungi Cinchonism Ergotism Lathyrism Locoism Mushrooms Strychnine 1 including venoms , toxins , foodborne illnesses .
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Acral Lentiginous Melanoma
Wikipedia
External links [ edit ] Classification D ICD - 10 : C43 ( ILDS C43.L60) ICD - 9-CM : 172.0 - 173.9 ICD-O : M8744/3 Scholia has a topic profile for Acral lentiginous melanoma . v t e Skin cancer of nevi and melanomas Melanoma Mucosal melanoma Superficial spreading melanoma Nodular melanoma lentigo Lentigo maligna / Lentigo maligna melanoma Acral lentiginous melanoma Amelanotic melanoma Desmoplastic melanoma Melanoma with features of a Spitz nevus Melanoma with small nevus-like cells Polypoid melanoma Nevoid melanoma Melanocytic tumors of uncertain malignant potential Nevus / melanocytic nevus Nevus of Ito / Nevus of Ota Spitz nevus Pigmented spindle cell nevus Halo nevus Pseudomelanoma Blue nevus of Jadassohn–Tièche Cellular Epithelioid Deep penetrating Amelanotic Malignant Congenital melanocytic nevus ( Giant Medium-sized Small-sized ) Balloon cell nevus Dysplastic nevus / Dysplastic nevus syndrome Acral nevus Becker's nevus Benign melanocytic nevus Nevus spilus v t e Medicine Specialties and subspecialties Surgery Cardiac surgery Cardiothoracic surgery Colorectal surgery Eye surgery General surgery Neurosurgery Oral and maxillofacial surgery Orthopedic surgery Hand surgery Otolaryngology ENT Pediatric surgery Plastic surgery Reproductive surgery Surgical oncology Transplant surgery Trauma surgery Urology Andrology Vascular surgery Internal medicine Allergy / Immunology Angiology Cardiology Endocrinology Gastroenterology Hepatology Geriatrics Hematology Hospital medicine Infectious disease Nephrology Oncology Pulmonology Rheumatology Obstetrics and gynaecology Gynaecology Gynecologic oncology Maternal–fetal medicine Obstetrics Reproductive endocrinology and infertility Urogynecology Diagnostic Radiology Interventional radiology Nuclear medicine Pathology Anatomical Clinical pathology Clinical chemistry Cytopathology Medical microbiology Transfusion medicine Other Addiction medicine Adolescent medicine Anesthesiology Dermatology Disaster medicine Diving medicine Emergency medicine Mass gathering medicine Family medicine General practice Hospital medicine Intensive care medicine Medical genetics Narcology Neurology Clinical neurophysiology Occupational medicine Ophthalmology Oral medicine Pain management Palliative care Pediatrics Neonatology Physical medicine and rehabilitation PM&R Preventive medicine Psychiatry Addiction psychiatry Radiation oncology Reproductive medicine Sexual medicine Sleep medicine Sports medicine Transplantation medicine Tropical medicine Travel medicine Venereology Medical education Medical school Bachelor of Medicine, Bachelor of Surgery Bachelor of Medical Sciences Master of Medicine Master of Surgery Doctor of Medicine Doctor of Osteopathic Medicine MD–PhD Related topics Alternative medicine Allied health Dentistry Podiatry Pharmacy Physiotherapy Molecular oncology Nanomedicine Personalized medicine Public health Rural health Therapy Traditional medicine Veterinary medicine Physician Chief physician History of medicine Book Category Commons Wikiproject Portal Outline
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Sternal Fracture
Wikipedia
Sternal fractures may also occur as a pathological fracture , in people who have weakened bone in their sternum, due to another disease process. [2] Sternal fracture can interfere with breathing by making it more painful; however, its primary significance is that it can indicate the presence of serious associated internal injuries, especially to the heart and lungs . [3] Contents 1 Signs and symptoms 1.1 Associated injuries 2 Causes 3 Diagnosis 4 Treatment 5 History 6 See also 7 References 8 External links Signs and symptoms [ edit ] Signs and symptoms include crepitus (a crunching sound made when broken bone ends rub together), [1] pain, tenderness , bruising , and swelling over the fracture site. [4] The fracture may visibly move when the person breathes, and it may be bent or deformed, [4] potentially forming a "step" at the junction of the broken bone ends that is detectable by palpation . [3] Associated injuries such as those to the heart may cause symptoms such as abnormalities seen on electrocardiograms. [1] The upper and middle parts of the sternum are those most likely to fracture, [5] but most sternal fractures occur below the sternal angle . [1] Associated injuries [ edit ] Because of the high frequency of associated injuries, clinicians are taught to suspect that a patient has multiple severe injuries if a sternal fracture is present. [4] Sternal fracture is commonly associated with injuries to the heart and lungs; if a person is injured with enough force to fracture the sternum, injuries such as myocardial and pulmonary contusions are likely. [1] Other associated injuries that may occur include damage to blood vessels in the chest, myocardial rupture , head and abdominal injuries , flail chest , [1] and vertebral fracture. [2] Sternal fractures may also accompany rib fractures and are high-energy enough injuries to cause bronchial tears (ruptures of the bronchioles ). [6] They may hinder breathing. [6] Due to the associated injuries, the mortality rate for people with sternal fracture is high, at an estimated 25–45%. [1] However, when sternal fractures occur in isolation, their outcome is very good. [7] There is controversy over the question of whether the presence of sternal fracture is an indication of cardiac injuries. [ citation needed ] Causes [ edit ] Illustration showing sternal fracture between ribs 3-4 Vehicle collisions are the usual cause of sternal fracture; [3] the injury is estimated to occur in about 3% of auto accidents. [8] The chest of a driver who is not wearing a seat belt may strike the steering wheel, and the shoulder component of a seatbelt may injure the chest if it is worn without the lap component. [3] It was common enough for the sternum to be injured by the seatbelt that it was included in the 'safety belt syndrome', [9] a pattern of injuries caused by seat belts in vehicle accidents. [10] The injury can also occur when the chest suddenly flexes, in the absence of an impact. [2] In the case of an injury sustained during CPR, the most common injuries sustained are rib fractures, with literature suggesting an incidence between 13% and 97%, and sternal fractures, with an incidence between 1% to 43%. [11] Additionally, injury to the sternum may be made more likely if there are other disease processes in place that have weakened the bone - in this case, the fracture that occurs is termed a pathologic fracture . [ citation needed ] Diagnosis [ edit ] CT scan showing a comminuted sternal fracture. [12] X-rays of the chest are taken in people with chest trauma and symptoms of sternal fractures, and these may be followed by CT scanning . [13] Since X-rays taken from the front may miss the injury, they are taken from the side as well. [14] Treatment [ edit ] Management involves treating associated injuries; people with sternal fractures but no other injuries do not need to be hospitalized. [4] However, because it is common for cardiac injuries to accompany sternal fracture, heart function is monitored with electrocardiogram. [15] Fractures that are very painful or extremely out of place can be operated on to fix the bone fragments into place, [4] but in most cases treatment consists mainly of reducing pain and limiting movement. [5] The fracture may interfere with breathing, requiring tracheal intubation and mechanical ventilation . [13] People who experience a pathologic fracture will be investigated for the cause of the underlying disease, if it is unknown.
- Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Recessive 1 Omim
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Cyst
Wikipedia
., MD, FACP, FACR. v t e Overview of tumors , cancer and oncology Conditions Benign tumors Hyperplasia Cyst Pseudocyst Hamartoma Malignant progression Dysplasia Carcinoma in situ Cancer Metastasis Primary tumor Sentinel lymph node Topography Head and neck ( oral , nasopharyngeal ) Digestive system Respiratory system Bone Skin Blood Urogenital Nervous system Endocrine system Histology Carcinoma Sarcoma Blastoma Papilloma Adenoma Other Precancerous condition Paraneoplastic syndrome Staging / grading TNM Ann Arbor Prostate cancer staging Gleason grading system Dukes classification Carcinogenesis Cancer cell Carcinogen Tumor suppressor genes / oncogenes Clonally transmissible cancer Oncovirus Carcinogenic bacteria Misc.PKD1, FLCN, PKD2, PRKD1, TP53, VEGFA, MMP9, PKHD1, CEACAM5, MLC1, MUC5B, PRKCSH, KRAS, PTEN, EXOC5, POSTN, GLUD1, COX1, MMP2, EGF, TPI1, UGDH, AR, CFTR, ANGPT2, IFNG, EPO, CRYL1, CDC42, HSF1, PAX2, CCL5, H6PD, CACNA1B, KIF3A, DICER1, BRCA1, PTGS1, CYP19A1, VIM, TSC1, TSC2, TULP3, VDAC1, TNS1, VEGFC, VIL1, VCAM1, AFP, TNF, SFTPC, PTH, RAG2, REN, RET, S100B, SCT, CCL11, SDHC, SELE, SLC9A1, TGFB1, SLC9A3, SLC12A2, SLC16A1, SST, CNTN2, PAX8, HNF1B, TERT, TFF2, XBP1, MVP, SEMA7A, KIZ, VANGL2, PRDM14, FKRP, MCPH1, PTGES2, DNAJC5, MINDY4, HS6ST2, MTDH, NLRP3, SLC9B2, ACTRT1, DAB2IP, LAMA1, TICAM2, MIR192, MIR223, SPAG11A, SNORA1, TMED7-TICAM2, H3P23, PARD3, POMGNT1, RNASET2, ANO1, BECN1, ADGRG1, HS6ST1, ATG5, MAGI2, WDR1, PDCD6IP, AKAP9, ABI2, SPAG11B, ZNRD2, DCTN6, PGRMC1, CORO1A, ARL6IP1, SMUG1, MCAT, PSMC3IP, TMED7, RNF43, RMND1, PTGER2, PGF, PTCH1, CLDN3, CRP, CST1, CTNNB1, CUX1, DAG1, EDN1, EPHA5, EPOR, ESR2, F2RL2, FBLN1, FGF7, FGF10, FLT1, NR5A1, GAD1, GDNF, GFAP, GNAS, GPER1, GPT, CLDN7, CLDN4, PSMD9, CNTF, AMH, BIRC3, BIRC5, APRT, AQP1, ARSA, AVP, BCHE, BCL2, BMI1, VPS51, CA9, CALB2, CAST, CASP3, CAV1, CD48, CDH8, CDKN1C, CDX2, CMD1B, HGF, HIF1A, HMMR, HOXA7, MCL1, MFAP1, MMP1, MMP7, MMP13, CYTB, ND1, MXI1, MYO5B, NT5E, OCRL, TNFRSF11B, PAK1, PAK2, PCOS1, PECAM1, ALDH1A3, PGR, ABCB1, PLXNA2, PRKCI, MCF2, EPCAM, LGALS4, IL5, HOXD13, HSPA4, ICAM1, IFI27, IFNA1, IFNA13, IGHA1, IL2, IL4, CXCR2, LAMB1, IL10, ITPR1, IVL, KRT6A, KRT13, KRT17, L1CAM, LAMA2, LAMA3, H3P47
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Alveolar Soft Part Sarcoma
Wikipedia
External links [ edit ] Classification D ICD - 10 : C49.9 ICD-O : M9581/3 OMIM : 606243 MeSH : D018234 External resources Orphanet : 163699 v t e Connective / soft tissue tumors and sarcomas Not otherwise specified Soft-tissue sarcoma Desmoplastic small-round-cell tumor Connective tissue neoplasm Fibromatous Fibroma / fibrosarcoma : Dermatofibrosarcoma protuberans Desmoplastic fibroma Fibroma / fibromatosis : Aggressive infantile fibromatosis Aponeurotic fibroma Collagenous fibroma Diffuse infantile fibromatosis Familial myxovascular fibromas Fibroma of tendon sheath Fibromatosis colli Infantile digital fibromatosis Juvenile hyaline fibromatosis Plantar fibromatosis Pleomorphic fibroma Oral submucous fibrosis Histiocytoma / histiocytic sarcoma : Benign fibrous histiocytoma Malignant fibrous histiocytoma Atypical fibroxanthoma Solitary fibrous tumor Myxomatous Myxoma / myxosarcoma Cutaneous myxoma Superficial acral fibromyxoma Angiomyxoma Ossifying fibromyxoid tumour Fibroepithelial Brenner tumour Fibroadenoma Phyllodes tumor Synovial -like Synovial sarcoma Clear-cell sarcoma Lipomatous Lipoma / liposarcoma Myelolipoma Myxoid liposarcoma PEComa Angiomyolipoma Chondroid lipoma Intradermal spindle cell lipoma Pleomorphic lipoma Lipoblastomatosis Spindle cell lipoma Hibernoma Myomatous general: Myoma / myosarcoma smooth muscle : Leiomyoma / leiomyosarcoma skeletal muscle : Rhabdomyoma / rhabdomyosarcoma : Embryonal rhabdomyosarcoma Sarcoma botryoides Alveolar rhabdomyosarcoma Leiomyoma Angioleiomyoma Angiolipoleiomyoma Genital leiomyoma Leiomyosarcoma Multiple cutaneous and uterine leiomyomatosis syndrome Multiple cutaneous leiomyoma Neural fibrolipoma Solitary cutaneous leiomyoma STUMP Complex mixed and stromal Adenomyoma Pleomorphic adenoma Mixed Müllerian tumor Mesoblastic nephroma Wilms' tumor Malignant rhabdoid tumour Clear-cell sarcoma of the kidney Hepatoblastoma Pancreatoblastoma Carcinosarcoma Mesothelial Mesothelioma Adenomatoid tumorASPSCR1, TFE3, MET, CD38, CD68, MLH1, MSH2, CTSK, CTNNB1, CSNK1D, ACTB, MYOD1, VEGFA, TP53, PAX8, TIMP2, SPG7, SET, VIM, XRCC1, CD163, TFEB, PROM1, PER2, PSMC2, NR1I3, TRIM13, PDPN, NES, ANGPTL2, BHLHE41, COG8, TRIM63, TMED6, RET, PCSK1, PSMA4, ATN1, ANG, APC, ARR3, ASS1, BSG, CALD1, CASR, CD34, CXADR, DES, MLANA, PRKAR1A, HIF1A, HTC2, ITGB1, KDR, MDK, MYOG, TBC1D25, ALDH1A1, PDGFRB, ABCB1, CXADRP1
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Hepatocellular Adenoma
Wikipedia
External links [ edit ] Classification D ICD-O : M8170/0 MeSH : D018248 DiseasesDB : 5726 External resources eMedicine : med/48 Orphanet : 54272 University of Utah—Pathology Images v t e Glandular and epithelial cancer Epithelium Papilloma / carcinoma Small-cell carcinoma Combined small-cell carcinoma Verrucous carcinoma Squamous cell carcinoma Basal-cell carcinoma Transitional cell carcinoma Inverted papilloma Complex epithelial Warthin's tumor Thymoma Bartholin gland carcinoma Glands Adenomas / adenocarcinomas Gastrointestinal tract: Linitis plastica Familial adenomatous polyposis pancreas Insulinoma Glucagonoma Gastrinoma VIPoma Somatostatinoma Cholangiocarcinoma Klatskin tumor Hepatocellular adenoma / Hepatocellular carcinoma Urogenital Renal cell carcinoma Endometrioid tumor Renal oncocytoma Endocrine Prolactinoma Multiple endocrine neoplasia Adrenocortical adenoma / Adrenocortical carcinoma Hürthle cell Other/multiple Neuroendocrine tumor Carcinoid Adenoid cystic carcinoma Oncocytoma Clear-cell adenocarcinoma Apudoma Cylindroma Papillary hidradenoma Adnexal and skin appendage sweat gland Hidrocystoma Syringoma Syringocystadenoma papilliferum Cystic, mucinous, and serous Cystic general Cystadenoma / Cystadenocarcinoma Mucinous Signet ring cell carcinoma Krukenberg tumor Mucinous cystadenoma / Mucinous cystadenocarcinoma Pseudomyxoma peritonei Mucoepidermoid carcinoma Serous Ovarian serous cystadenoma / Pancreatic serous cystadenoma / Serous cystadenocarcinoma / Papillary serous cystadenocarcinoma Ductal, lobular, and medullary Ductal carcinoma Mammary ductal carcinoma Pancreatic ductal carcinoma Comedocarcinoma Paget's disease of the breast / Extramammary Paget's disease Lobular carcinoma Lobular carcinoma in situ Invasive lobular carcinoma Medullary carcinoma Medullary carcinoma of the breast Medullary thyroid cancer Acinar cell Acinic cell carcinoma v t e Digestive system neoplasia GI tract Upper Esophagus Squamous cell carcinoma Adenocarcinoma Stomach Gastric carcinoma Signet ring cell carcinoma Gastric lymphoma MALT lymphoma Linitis plastica Lower Small intestine Duodenal cancer Adenocarcinoma Appendix Carcinoid Pseudomyxoma peritonei Colon/rectum Colorectal polyp : adenoma , hyperplastic , juvenile , sessile serrated adenoma , traditional serrated adenoma , Peutz–Jeghers Cronkhite–Canada Polyposis syndromes: Juvenile MUTYH-associated Familial adenomatous / Gardner's Polymerase proofreading-associated Serrated polyposis Neoplasm: Adenocarcinoma Familial adenomatous polyposis Hereditary nonpolyposis colorectal cancer Anus Squamous cell carcinoma Upper and/or lower Gastrointestinal stromal tumor Krukenberg tumor (metastatic) Accessory Liver malignant : Hepatocellular carcinoma Fibrolamellar Hepatoblastoma benign : Hepatocellular adenoma Cavernous hemangioma hyperplasia : Focal nodular hyperplasia Nodular regenerative hyperplasia Biliary tract bile duct : Cholangiocarcinoma Klatskin tumor gallbladder : Gallbladder cancer Pancreas exocrine pancreas : Adenocarcinoma Pancreatic ductal carcinoma cystic neoplasms : Serous microcystic adenoma Intraductal papillary mucinous neoplasm Mucinous cystic neoplasm Solid pseudopapillary neoplasm Pancreatoblastoma Peritoneum Primary peritoneal carcinoma Peritoneal mesothelioma Desmoplastic small round cell tumorHNF1A, A2M, CTNNB1, HRAS, NR1I3, PTEN, CDKN1B, UBE2E2, TMEM70, KRAS, PTPN11, HP, CYP2E1, CARM1, HNF4A, APPL1, INS, PDX1, KCNJ11, ABCC8, KLF11, NEUROD1, CEL, PAX4, BLK, PHKA2, GCK, PHKG2, PRKAR1A, G6PC, GLUL, IL6ST, LRPPRC, NM, SLC37A4, TCF7, ASS1, HCA1, LOC110806263, TP53, STAT3, GOT2, HCC, CYP1B1, TERT, CRP, MST1, FABP1, CDKN2A, GPC3, SYCE1L, KLHL1, MIR130B, RSPO2, GADL1, AZIN2, LMLN, PERCC1, TMPRSS13, TGFB1, ABCC3, PDGFC, LGR5, UGT2B7, WNT1, TRPV2, MLXIPL, HEBP1, BHLHE22, CNBP, SLBP, STAM2, SSTR2, LATS1, A1BG, SREBF1, AZU1, CYP3A4, CYP2B7P, CYP2B6, CYP1A2, MAP3K8, ABCC2, CCND2, APC, EGF, ANXA2, ALDH3A1, ALB, AKT1, AFP, ACTB, AOC1, EEF1B2P2, FXN, SPTBN2, MET, SPTB, SHBG, SAA2, SAA1, NOTCH2, NFE2L2, MSMB, IL6, FRK, IL1RN, IGF2R, HMGB1, HDLBP, GFAP, GABPA, MTOR, MTHFR
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Malonyl-Coa Decarboxylase Deficiency
Wikipedia
External links [ edit ] Malonyl-CoA decarboxylase deficiency at NLM Genetics Home Reference Classification D ICD - 10 : E72.8 OMIM : 248360 MeSH : C535702 DiseasesDB : 33804 External resources Orphanet : 943 v t e Inborn error of lipid metabolism : fatty-acid metabolism disorders Synthesis Biotinidase deficiency (BTD) Degradation Acyl transport Carnitine CPT1 CPT2 CDSP CACTD Adrenoleukodystrophy (ALD) Beta oxidation General Acyl CoA dehydrogenase Short-chain SCADD Medium-chain MCADD Long-chain 3-hydroxy LCHAD Very long-chain VLCADD Mitochondrial trifunctional protein deficiency (MTPD): Acute fatty liver of pregnancy Unsaturated 2,4 Dienoyl-CoA reductase deficiency (DECRD) Odd chain Propionic acidemia (PCC deficiency) Other 3-hydroxyacyl-coenzyme A dehydrogenase deficiency (HADHD) Glutaric acidemia type 2 (MADD) To acetyl-CoA Malonic aciduria (MCD) Aldehyde Sjögren–Larsson syndrome (SLS) v t e Medicine Specialties and subspecialties Surgery Cardiac surgery Cardiothoracic surgery Colorectal surgery Eye surgery General surgery Neurosurgery Oral and maxillofacial surgery Orthopedic surgery Hand surgery Otolaryngology ENT Pediatric surgery Plastic surgery Reproductive surgery Surgical oncology Transplant surgery Trauma surgery Urology Andrology Vascular surgery Internal medicine Allergy / Immunology Angiology Cardiology Endocrinology Gastroenterology Hepatology Geriatrics Hematology Hospital medicine Infectious disease Nephrology Oncology Pulmonology Rheumatology Obstetrics and gynaecology Gynaecology Gynecologic oncology Maternal–fetal medicine Obstetrics Reproductive endocrinology and infertility Urogynecology Diagnostic Radiology Interventional radiology Nuclear medicine Pathology Anatomical Clinical pathology Clinical chemistry Cytopathology Medical microbiology Transfusion medicine Other Addiction medicine Adolescent medicine Anesthesiology Dermatology Disaster medicine Diving medicine Emergency medicine Mass gathering medicine Family medicine General practice Hospital medicine Intensive care medicine Medical genetics Narcology Neurology Clinical neurophysiology Occupational medicine Ophthalmology Oral medicine Pain management Palliative care Pediatrics Neonatology Physical medicine and rehabilitation PM&R Preventive medicine Psychiatry Addiction psychiatry Radiation oncology Reproductive medicine Sexual medicine Sleep medicine Sports medicine Transplantation medicine Tropical medicine Travel medicine Venereology Medical education Medical school Bachelor of Medicine, Bachelor of Surgery Bachelor of Medical Sciences Master of Medicine Master of Surgery Doctor of Medicine Doctor of Osteopathic Medicine MD–PhD Related topics Alternative medicine Allied health Dentistry Podiatry Pharmacy Physiotherapy Molecular oncology Nanomedicine Personalized medicine Public health Rural health Therapy Traditional medicine Veterinary medicine Physician Chief physician History of medicine Book Category Commons Wikiproject Portal Outline
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Pain Disorder
Wikipedia
"Aftermath of sexual abuse history on adult patients suffering from chronic functional pain syndromes: an fMRI pilot study". J Psychosom Res . 68 (5): 483–7. doi : 10.1016/j.jpsychores.2010.01.020 .
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Blastoma
Wikipedia
In most cases, HBL is an sporadic pathology, although it has been sometimes associated with specific genetic abnormalities such as the Beckwith-Wiedemann syndrome and familial adenomatous polyposis.
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Acquired Haemophilia
Wikipedia
These autoantibodies constitute the most common spontaneous inhibitor to any coagulation factor and may induce spontaneous bleeding in patients with no previous history of a bleeding disorder. [1] Its incidence is approximately 1.5 cases/million/year. [2] The distribution is bimodal with a first period occurrence between 20 and 30 years old, which mainly corresponds to women who develop this disorder in the postpartum, and a second peak between 68 and 80 years old, corresponding to the majority of patients, with no sex difference. [3] An underlying medical condition can be identified in up to 50% of patients, including cancer either solid or hematologic; autoimmune diseases such as rheumatoid arthritis , Sjögren’s syndrome , or bullous pemphigoid ; administration of drugs and pregnancy .
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Spinocerebellar Ataxia, Autosomal Recessive 8
Omim
The finding of 5 different mutations in a relatively homogeneous population led Gros-Louis et al. (2007) to predict that mutations in the SYNE1 gene may be responsible for a substantial fraction of all adult-onset autosomal recessive ataxia syndromes with cerebellar atrophy. Dupre et al. (2007) identified 2 additional SYNE1 mutations (608441.0006; 608441.0007) in French Canadian patients with SCAR8.
- Neuropathy, Hereditary Motor And Sensory, Type Vib, With Optic Atrophy Omim
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Bipolar Disorder
Wikipedia
Even when family and friends recognize mood swings , the individual will often deny that anything is wrong. [34] If not accompanied by depressive episodes, hypomanic episodes are often not deemed problematic, unless the mood changes are uncontrollable, or volatile. [32] Most commonly, symptoms continue for a few weeks to a few months. [35] Depressive episodes Main article: Major depressive disorder 'Melancholy' by William Bagg , after a photograph by Hugh Welch Diamond Symptoms of the depressive phase of bipolar disorder include persistent feelings of sadness , irritability or anger, loss of interest in previously enjoyed activities , excessive or inappropriate guilt , hopelessness , sleeping too much or not enough , changes in appetite and/or weight, fatigue , problems concentrating, self-loathing or feelings of worthlessness, and thoughts of death or suicide . [36] Although the DSM-5 criteria for diagnosing unipolar and bipolar episodes are the same, some clinical features are more common in the latter, including increased sleep, sudden onset and resolution of symptoms, significant weight gain or loss, and severe episodes after childbirth. [12] The earlier the age of onset, the more likely the first few episodes are to be depressive. [37] For most people with bipolar types 1 and 2, the depressive episodes are much longer than the manic or hypomanic episodes. [17] Since a diagnosis of bipolar disorder requires a manic or hypomanic episode, many affected individuals are initially misdiagnosed as having major depression and incorrectly treated with prescribed antidepressants. [38] Mixed affective episodes Main article: Mixed affective state In bipolar disorder, a mixed state is an episode during which symptoms of both mania and depression occur simultaneously. [39] Individuals experiencing a mixed state may have manic symptoms such as grandiose thoughts while simultaneously experiencing depressive symptoms such as excessive guilt or feeling suicidal. [39] They are considered to have a higher risk for suicidal behavior as depressive emotions such as hopelessness are often paired with mood swings or difficulties with impulse control . [39] Anxiety disorders occur more frequently a comorbidity in mixed bipolar episodes than in non-mixed bipolar depression or mania. [39] Substance abuse (including alcohol ) also follows this trend, thereby appearing to depict bipolar symptoms as no more than a consequence of substance abuse. [39] Comorbid conditions The diagnosis of bipolar disorder can be complicated by coexisting ( comorbid ) psychiatric conditions including obsessive-compulsive disorder , substance-use disorder , eating disorders , attention deficit hyperactivity disorder , social phobia , premenstrual syndrome (including premenstrual dysphoric disorder ), or panic disorder . [31] [36] [40] [41] A thorough longitudinal analysis of symptoms and episodes, assisted if possible by discussions with friends and family members, is crucial to establishing a treatment plan where these comorbidities exist. [42] Children of parents with bipolar disorder more frequently have other mental health problems. [ needs update ] [43] People with bipolar disorder often have other co-existing psychiatric conditions such as anxiety (present in about 71% of people with bipolar disorder), substance use (56%), personality disorders (36%) and attention deficit hyperactivity disorder (10–20%) which can add to the burden of illness and worsen the prognosis. [17] Certain medical conditions are also more common in people with bipolar disorder as compared to the general population. This includes increased rates of metabolic syndrome (present in 37% of people with bipolar disorder), migraine headaches (35%), obesity (21%) and type 2 diabetes (14%). [17] This contributes to a risk of death that is two times higher in those with bipolar disorder as compared to the general population. [17] Causes The causes of bipolar disorder likely vary between individuals and the exact mechanism underlying the disorder remains unclear. [44] Genetic influences are believed to account for 73–93% of the risk of developing the disorder indicating a strong hereditary component. [10] The overall heritability of the bipolar spectrum has been estimated at 0.71. [45] Twin studies have been limited by relatively small sample sizes but have indicated a substantial genetic contribution, as well as environmental influence. ... Infectious causes of mania that may appear similar to bipolar mania include herpes encephalitis , HIV , influenza , or neurosyphilis . [83] Certain vitamin deficiencies such as pellagra ( niacin deficiency), Vitamin B12 deficiency , folate deficiency , and Wernicke Korsakoff syndrome ( thiamine deficiency ) can also lead to mania. [83] Common medications that can cause manic symptoms include antidepressants, prednisone , Parkinson's disease medications, thyroid hormone , stimulants (including cocaine and methamphetamine), and certain antibiotics . [94] Bipolar spectrum Since Emil Kraepelin's distinction between bipolar disorder and schizophrenia in the 19th century, researchers have defined a spectrum of different types of bipolar disorder. ... One third of people with BD remain unemployed for one year following a hospitalization for mania. [145] Depressive symptoms during and between episodes, which occur much more frequently for most people than hypomanic or manic symptoms over the course of illness, are associated with lower functional recovery in between episodes, including unemployment or underemployment for both BD-I and BD-II. [5] [146] However, the course of illness (duration, age of onset, number of hospitalizations, and presence or not of rapid cycling) and cognitive performance are the best predictors of employment outcomes in individuals with bipolar disorder, followed by symptoms of depression and years of education. [146] Recovery and recurrence A naturalistic study from first admission for mania or mixed episode (representing the hospitalized and therefore most severe cases) found that 50% achieved syndromal recovery (no longer meeting criteria for the diagnosis) within six weeks and 98% within two years. ... However, 40% went on to experience a new episode of mania or depression within 2 years of syndromal recovery, and 19% switched phases without recovery. [147] Symptoms preceding a relapse ( prodromal ), specially those related to mania, can be reliably identified by people with bipolar disorder. [148] There have been intents to teach patients coping strategies when noticing such symptoms with encouraging results. [149] Suicide Bipolar disorder can cause suicidal ideation that leads to suicide attempts.HTR2A, S100B, ANK3, CACNA1C, COMT, NCAN, SP4, ADCY2, POLG, FADS2, LMAN2L, GAD1, GSK3B, SLC6A4, DRD1, BDNF, ITIH1, CLOCK, NR3C1, MTHFR, NDUFV2, GRIN2A, RELN, ACE, GRK3, PDE4B, DRD5, SNAP25, ATP1A3, CAMK2A, TACR1, NTRK2, POU3F2, POMC, INS, AKR1C4, BHLHE40, GRIK2, SERPINA1, NTNG2, NRG1, ZNF804A, DGKH, CHRNA7, TENM4, SYNE1, TCF4, ATP2A2, SLC25A4, PBRM1, CACNB2, TRANK1, PDE10A, CSMD1, NFIX, TSPAN8, LINC02694, TCF7L2, NLGN1, PALB2, ITIH3, SEC24C, FEZ1, ZCCHC2, P2RX7, RPS6KA2, TH, XBP1, TNF, RIMS1, PACS1, SLC6A3, MAOA, CD47, DRD3, DRD2, SCN2A, DAOA, TPH2, STARD9, IL6, SHANK2, DISC1, NEK4, ADD3, PC, SSBP2, HDAC5, THSD7A, IMPA2, AKT1, GRIN2B, PDLIM5, DRD4, FKBP5, DTNBP1, HTR2C, ARNTL, TRPM2, ERDA1, KCNN3, SLC1A2, BRD1, IL1B, WFS1, CSNK1E, DAO, TPH1, HTR1A, PPP1R1B, GRIK4, BCL2, PER3, ST8SIA2, DAOA-AS1, IGFBP2, PLA2G1B, PVALB, GRM3, MIR137, TIMELESS, RGS4, GRN, APOE, DUSP6, PON1, DDC, ALDH2, RORA, GRIN1, NCAM1, GPR50, IGF1, NR4A2, MMP9, TSNAX, GPRC5D, SLC6A2, HTR3B, SYNGR1, PIP4K2A, GDNF, TSPO, CXCL8, IMPA1, ESR1, NR1D1, INPP1, ADCYAP1, HPGDS, MAPK1, HSP90B1, GABRA5, GABRA3, G6PD, ERBB4, DPYSL2, HTR3A, CRHR1, SYN2, CALB1, TLR2, SIRT1, NOTCH4, DBH, AVPR1B, GRM7, YWHAZ, CHRFAM7A, DLG3, CREB1, SOD1, TLR4, GRM5, GRIK1, DNAJB1, PRKCI, PTPA, ITPR1, MC2R, PSEN2, HTR1B, HSPA5, HSPA4, PFKL, NOS3, GRIA3, FYN, GNAL, PROKR2, HLA-G, SORCS2, NPAS2, GSTM1, GRIA2, HTR5A, IL1RN, PCNT, NRGN, PLA2G2A, GFAP, NTF3, PLA2G4A, GCH1, GSTT1, GRIA1, SLC12A6, MIR212, SLC18A2, SST, PGP, CTLA4, WHRN, CRY1, CRH, NCS1, CNR2, CNR1, CHRNB3, CUX2, VIP, YWHAE, CALCA, CACNA1D, BCR, PLA2G6, BAG1, NAPG, TSNAX-DISC1, ASMT, PER2, NRG3, NDST3, NRXN1, ADRB2, ADCY8, ADARB1, RASGRP1, SOD2, KCNQ2, SAT1, SLC1A3, KCNQ3, RFX4, ANKK1, MDGA1, EGR2, S100A10, EGR3, F9, FABP7, DCLK1, NPAS3, MMP10, VAPA, MAGI1, HIP1R, MTHFD1, REN, ABCB1, ND1, PSPN, MMP3, MTR, RTN4, CNTN6, PREP, IFT27, KLK8, AKAP10, ATF5, NTNG1, VAMP3, NR3C2, PCLO, GPRIN2, HMGXB4, MPPE1, MAGI2, USP46, TOM1, RAPGEF5, ERVW-1, RNF41, MAOB, ZDHHC8, MC5R, CLEC10A, TSHZ1, DBNL, NCOR2, CARTPT, RARA, LHX5, MFGE8, HCG9, RASGRF1, NOD2, TRPC7, FZD4, SLC17A6, TAC1, NR2E1, LARS2, ST3GAL1, TLL2, TGM2, AHI1, SEZ6L, TDO2, SLC1A4, PAH, PAWR, NDUFV1, SRRT, VAMP2, CNTNAP2, SSTR5, PIK3C3, SPR, PDE4A, SLC18A1, PDYN, SMS, DOCK9, PI4K2B, OTX2, IMPACT, GPR78, PGAM1, SYN3, STAB1, NEDD4, SLC17A7, MLC1, DOK5, NNMT, MBD5, YWHAH, SCN8A, PLCG1, VGF, VEGFA, VDR, PTGDS, UCP2, CCL2, TRPC3, TPO, SLC39A3, TGFB1, MBL2, FKBP1A, BCL9, ABCA13, ALOX12, BID, PPIEL, HLA-DRB1, BRCA2, ERBB3, C9orf72, AGT, SLC22A16, GRK2, S1PR1, AFG1L, DSCAM, MCHR2, DCTN5, FGFR1, BCHE, DNAH8, AVP, CBLIF, GLO1, ATF4, GRIN3A, APOD, MCHR1, GABRB3, GRIA4, GRIK3, GABRB2, GABRB1, GABRA1, FMR1, FOXO3, ATP1A2, GSTZ1, MIR2682, DNMT1, SP8, CSNK1D, CASP8, MIR206, IFNG, TAAR6, ACTB, CCKAR, CRHBP, CSRP1, CALM2, ADRA2C, CRY2, CBS, ISL1, ITGA9, CRHR2, IFNA1, ITGAM, DIO2, CHRM2, DLX1, DLG4, CHRM3, GABRR2, ARRB2, PRODH, PMCH, GAP43, CHRNA2, HCAR3, FOXP3, CDH17, PPP2R2C, FGF17, TSHB, GAD2, PRKCZ, PLCXD3, GABRG1, GAL, GABRR1, CDH7, PPID, PLEKHO1, PPP3CC, CACNA1B, ATP1A1, SRSF3, CACNA1A, SLC6A13, DLG2, FGF20, SLC5A3, SLC1A6, FBXL3, EHHADH, SLC1A1, SRPK2, DAZAP1, CPLX2, SFRP1, PHETA1, CACNG5, DKK4, CALR, PLCB1, DBN1, ASTN2, BDKRB2, DGKB, VIPR2, CNTN4, STK4, FGFR2, CPLX1, PPARD, BHLHE41, ME2, HLA-DRB4, ULK4, LBX1, NDUFV3, ITIH4, RACK1, GLYAT, NEFM, MAP2, NEFL, IL2RB, HLA-E, MLLT3, ZNF592, ROR1, ADM, NTRK1, ARHGEF10, HIF1A, HINT1, SEPTIN11, DIXDC1, GSK3A, GRM4, TUBA8, KCTD12, ADRA1A, CHRNA6, MRPS33, ADCY3, FSTL5, PFKFB3, ACADS, HTR4, LDHA, PDE9A, GNB3, AKT2, CHMP1B, TMSB10, GNB1L, GRID1, ARNTL2, GRIK5, C14orf28, PIP4K2C, APP, MAD1L1, CAMKMT, FXR1, MKLN1, ABCG1, PRR5-ARHGAP8, HLA-A, EGFR, SESTD1, MECP2, CACNB3, ASCC2, MYO5B, CNNM2, SOX2-OT, FADS1, LAMP3, LINC00461, MMADHC-DT, LHFPL3-AS1, TSBP1-AS1, SDCCAG8, ADCY1, LINC00243, DMTF1, LINC01748, LINC02033, CDC25B, MIR137HG, LINC01643, LINC01121, LINC02822, TRAF3IP2-AS1, JADE2, HDAC9, HIRA, RPRD2, UFD1, LINC02109, DOCK4, SMIM4, LINC01470, LAMA4-AS1, ATP2B2, POLG2, NUMB, TAF9BP2, AMPD3, CTSF, BORCS7-ASMT, TLCD4-RWDD3, EBNA1BP2, RERE, ACTL7A, LINC02384, ALOX12-AS1, TSBP1, USP8, IQCH-AS1, PROM1, MAU2, ASAP2, ARVCF, MGAT4A, ALOX12P2, BABAM2, CUL4A, TRIM26, MRPL33, DDN, KCNMB2, AKAP6, RASAL2, CUBN, LINC01592, FER1L6, KMT2D, SLC25A17, IPO8, IGSF9B, NT5C2, LINC01358, ARHGEF15, SLC8A1-AS1, CMAHP, SPTLC1, SFTA2, FA2H, CEP85L, PDE3B, GLT8D1, HLF, WDR12, HLA-DMB, HLA-DMA, ATP6V1E2, GULOP, RNLS, CABLES1, GSS, ARHGEF10L, RASIP1, TMEM132C, PGAP3, PCDH12, CSMD2, KDM3B, MPP6, SLC25A26, GP1BB, PIK3C2A, GFRA2, MTERF4, PLCB4, MUCL3, PHF7, NEK7, MACROD2, TWNK, NFYC, ANKS1B, KIF15, BCL11B, LMO7, STT3A, IQCH, DEPTOR, GIGYF1, C11orf80, MCTP1, GRTP1, CARF, RBKS, CDH23, CCDC102B, CCDC170, GRAMD1B, AS3MT, UXS1, SPG11, TMPRSS5, SLC4A10, SMIM8, ZNF93, ZCCHC7, ZNF577, PARP10, NFIA, CGNL1, COMMD10, FAM178B, LHFPL3, DNMT3A, SMPD1, GSDME, ZBTB20, ZNF740, MYO1H, TRPC4AP, MYRF-AS1, LTN1, KSR2, SNED1, FAM177A1, INTS7, TTLL6, ARHGAP8, CRP, TBX1, ZNF615, TCF3, DCBLD1, TRIM42, SEC11A, GRIP1, RFESD, ZFPM2, SLC35F4, TLE4, CLCN4, SLIT1, CADM2, KLHL23, SPCS1, RRM2B, ZNRD1, CPNE8, FLI1, PTPRG, PTS, C11orf21, MACROD1, CDAN1, TLCD4, RARRES2, CFAP57, RASGRF2, GNL3, PCDH15, FBLN1, RBMS3, RPN2, FER1L6-AS2, RPS6KA3, OTUD7A, RREB1, RXRG, PRSS35, ADAMTS16, ERBB2, STX2, JMJD1C, ASCC1, H3P40, NFKB1, ARHGEF7, CD40, EIF4EBP1, NOS1, DLX4, IL1A, LEP, NOS2, SHANK3, LOC110806262, CTNNB1, MIR34A, TMTC1, MAFD2, GPRC5C, MDD1, MZB1, ADIPOQ, CACNG2, PLB1, FAAH, BPI, STIN2-VNTR, FGF9, PRPF6, GRB2, HRAS, NGF, ACACA, BDNF-AS, CCK, THOP1, TLR1, COX2, PTPN5, HLA-C, CAT, IL4, EXOSC6, NLRP3, CYP2D6, FAT1, ETV5, HDGFL3, EPHB2, PTGS2, PGC, MINDY2, IL10, P2RY2, DISC2, CD36, P2RY1, P2RX5, P2RX4, P2RX3, P2RX1, RASSF7, CXCR3, NRAS, SHC4, NR4A3, ACSL4, KMO, PDLIM7, SYNJ1, FASTK, FTO, HOMER1, PPARGC1A, ENDOU, MAFD6, HTR1F, KL, IL18R1, P2RX5-TAX1BP3, P2RX6, NPL, APOB, MAFD4, MAFD1, MIR708, MTCO2P12, PLA2G10, EBI3, CAMKK2, HSPD1, BMS1, P2RX2, MSMB, LINC00273, SLITRK2, GDF10, IDH3A, GPR151, IDH2, FLAD1, GATA3, GC, PWAR1, BPIFA2, SVEP1, PPM1K, EHMT1, IGHG3, IFNA13, CKAP2L, FKBP1AP1, FKBP1AP2, GALC, FKBP1AP3, BICC1, IDH3B, PNPLA3, FKBP1AP4, FUT3, PPP1R2C, MRGPRX4, RBM45, GLP1R, HPT, HSPE1, HPN, HMGB1, LMLN, HSPG2, HCRT, HTC2, HTR1E, HBA2, TMPRSS13, MIXL1, HBA1, GTF2A1, PARP9, GRM1, HTR6, NDEL1, HTR7, GPX3, IDH1, FBXO32, GPER1, UTS2R, MRGPRX3, HSPA1L, TWIST2, GOT2, GNAZ, HLA-DRA, DGCR2, KCTD7, CAV2, FAS-AS1, LINC00271, ATP1B3, C20orf181, OPN1SW, PSS, OIP5-AS1, CA5A, CALM1, CALM3, CAMP, SCZD12, MIR504, MIR497, MIR346, GPR166P, VN1R17P, CAV1, NPIPB7, TNFSF12-TNFSF13, MIR29C, ASTN1, SCZD13, BACE1-AS, ADCYAP1R1, ASIC2, ACO1, ACO2, THRA1/BTR, TEMPS, TPTEP2-CSNK1E, ACP1, ACTA2, ADCY9, ADORA1, FAS, AGRP, ALAS1, CCAT2, AMD1, AMPH, ANG, SLC25A6, APOA1, LINC01672, MIR223, MIR195, F2R, MIR184, CSF2, HCCAT5, CUX1, DDIT3, OR10A4, DNMT3B, DNTT, MRGPRX1, LRRC57, DPYS, DRP2, DUSP2, GPRC6A, EGR1, OPN5, ZUP1, EPO, ESR2, OXER1, KANK4, EVC, ENDOV, CRMP1, ZNF493, CEACAM5, MIR149, MIR146A, MIR144, KRIT1, MIR132, PHOBS, CD14, CDH13, CDSN, CHI3L1, CPOX, CISH, CCR5, NANOS3, GOLGA6A, COL2A1, GADL1, COL9A3, KLF6, COX8A, DEFB1, SCZD10, IL18, TGFB2, PART1, TPSG1, QPCT, TBC1D22A, ADAM17, TAGLN, TERT, SMUG1, LPAR3, TG, THRA, RPL29, TLR5, TNR, TP53, TPI1, TSHR, RPGRIP1L, TYR, ADGRL3, ANKRD12, UBC, SYP, VAMP7, SOSTDC1, SH2B1, RPS23, IL17C, S100A11, CYTH4, SCD, SDHC, SGCG, SND1, HAVCR1, ST3GAL3, PMEL, SORL1, SOS1, SREBF2, ST13, STAR, STAT1, STAT5A, SS18L1, STAT5B, STXBP3, VRK2, VTN, CXCR4, UTS2, NR1I2, CHL1, WASF1, ZMYM3, ARID3B, MTA2, KAT5, CAP2, COX5A, PPIE, MICU1, TLR6, SIGMAR1, LITAF, GDF15, RIDA, BAG3, SOCS5, NOS1AP, CEBPZ, SART3, HPSE, RAB40B, ARHGEF5, RIPK2, MAPK8IP3, TBC1D9, VWA8, TAF15, SLC14A2, TPX2, BRAP, FZD7, ZNF365, FNDC3A, PKP4, PDLIM4, COPE, PARK7, SCN11A, PSMG1, SOCS1, TNFSF12, NISCH, CIT, TNFSF10, PCDH17, RORB, INSRR, NDUFS1, SEMA6A, LRRC7, NUFIP2, MST1, COX1, ND4, MTNR1B, MTRR, MUSK, NDUFA6, NFATC3, RIT2, NFE2L2, DTWD1, NFKB2, NGFR, PCDHA1, SNU13, NHS, NOTCH3, ATF7IP, NPTX1, DPP10, LRRC4C, MAGEE1, HAMP, ITGB4, MCPH1, SLC52A2, ITGB5, ITPR3, POGLUT2, KIF22, LAMC2, LMX1A, ETNPPL, MARCKS, MXD1, HHIP, MEN1, MMP2, MMP16, MRC1, MS, NR1H4, PROK2, LGR6, PPP1R9A, KLK15, TRPV6, BFAR, HSPA14, PPP3CB, PRKAR1A, MAPK3, PRNP, PDE11A, DHH, ITSN2, PRS, PSD, PSPH, OBP2A, PTGS1, RAC1, RAP1A, RAPSN, RBM3, REM1, IGKV2D-28, REG1A, RABGEF1, PPARG, POU3F1, OAS3, NRN1, CHDH, OPRM1, OXTR, PACC1, RCBTB1, TUG1, CASZ1, BIVM, REG3A, PDE2A, TERF2IP, CNTN5, PTOV1, SERPINF1, PENK, CFP, PIK3CA, CINP, PLXNA2, POR, SNX7, ABO
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Lmna-Related Dilated Cardiomyopathy
Gene_reviews
The following are also common: Symptomatic bradyarrhythmias requiring cardiac pacemakers Supraventricular arrhythmias including atrial flutter, atrial fibrillation, supraventricular tachycardia, and the sick sinus syndrome (i.e., tachycardia-bradycardia syndrome) Ventricular arrhythmias including frequent premature ventricular contractions (PVCs), ventricular tachycardia, and ventricular fibrillation Sudden cardiac death may occur with progressive disease.