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Primary Carnitine Deficiency
Medlineplus
This disorder is sometimes mistaken for Reye syndrome, a severe disorder that may develop in children while they appear to be recovering from viral infections such as chicken pox or flu. Most cases of Reye syndrome are associated with the use of aspirin during these viral infections.SLC22A5, CACNA1C, UBIAD1, MIR3936HG, TBX6, DLL3, SCD, HES7, TGFB1, TK2, BRAP, MADD, WASF1, ZFYVE9, WASF2, DMRT2, TMLHE, ABHD5, SFTPD, SAR1A, CHPT1, PNPLA2, CDH23, SCD5, RIPPLY2, MESP2, BEAN1, DAGLB, CHKB-CPT1B, SLC22A4, ACADM, APOB, RYR1, ARG1, DAGLA, CNR1, CPT1A, CPT1B, CPT2, CSF2, CD55, DBH, ETFA, ETFB, ETFDH, FAAH, GPT, GZMM, HBB, HMGCR, IMPA1, INSIG1, LAMC2, LFNG, MBL2, KMT2A, SERPINE1, PDK4, RN7SL263P
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Angel Wing
Wikipedia
A duck with angel wing A Muscovy duck with angel wing Angel wing , also known as airplane wing , [1] slipped wing , crooked wing , and drooped wing , is a syndrome that affects primarily aquatic birds, such as geese and ducks , in which the last joint of the wing is twisted with the wing feathers pointing out laterally, instead of lying against the body. ... It has also been reported in goshawks , bustard chicks, and psittacine birds ( budgerigars , macaws , and conures ). [2] The syndrome is acquired in young birds. Due to a high- calorie diet, especially one high in proteins and/or low in vitamin D , vitamin E , and manganese , one or both carpus (wrist) joints are delayed in their development relative to the rest of the wing; for reasons unknown, if only one wing is affected, it is usually the left one.
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Prurigo Pigmentosa
Wikipedia
External links [ edit ] Classification D ICD - 10 : L28.2 ( ILDS L28.226) v t e Dermatitis and eczema Atopic dermatitis Besnier's prurigo Seborrheic dermatitis Pityriasis simplex capillitii Cradle cap Contact dermatitis ( allergic , irritant ) plants: Urushiol-induced contact dermatitis African blackwood dermatitis Tulip fingers other: Abietic acid dermatitis Diaper rash Airbag dermatitis Baboon syndrome Contact stomatitis Protein contact dermatitis Eczema Autoimmune estrogen dermatitis Autoimmune progesterone dermatitis Breast eczema Ear eczema Eyelid dermatitis Topical steroid addiction Hand eczema Chronic vesiculobullous hand eczema Hyperkeratotic hand dermatitis Autosensitization dermatitis / Id reaction Candidid Dermatophytid Molluscum dermatitis Circumostomy eczema Dyshidrosis Juvenile plantar dermatosis Nummular eczema Nutritional deficiency eczema Sulzberger–Garbe syndrome Xerotic eczema Pruritus / Itch / Prurigo Lichen simplex chronicus / Prurigo nodularis by location: Pruritus ani Pruritus scroti Pruritus vulvae Scalp pruritus Drug-induced pruritus Hydroxyethyl starch-induced pruritus Senile pruritus Aquagenic pruritus Aquadynia Adult blaschkitis due to liver disease Biliary pruritus Cholestatic pruritus Prion pruritus Prurigo pigmentosa Prurigo simplex Puncta pruritica Uremic pruritus Other substances taken internally: Bromoderma Fixed drug reaction Nummular dermatitis Pityriasis alba Papuloerythroderma of Ofuji This cutaneous condition article is a stub .
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Caprine Arthritis Encephalitis
Wikipedia
The disease is found worldwide. [1] Two syndromes of CAE occur. Adult goats develop a chronic progressive arthritis , whereas young goats develop a neurological syndrome, with signs of paresis or paralysis . [1] Less commonly, mastitis or pneumonia may occur. [1] Infection is life-long, and it may be years before signs of the disease occur. [2] The reason for the long (and variable) period of dormancy of the virus is not known. [3] In goats which develop arthritis, the joints become inflamed and swollen, and the goats will slowly lose condition. [4] In some cases the goat will not be able to stand.
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Ulcerative Dermal Necrosis
Wikipedia
ISBN 9780412321405 . v t e Fish diseases and parasites Pathogens Aeromonas salmonicida Nervous necrosis virus Columnaris Enteric redmouth Fin rot Fish dropsy Flavobacterium Hematopoietic necrosis Heterosigma akashiwo Hole in the head Hypodermal and hematopoietic necrosis Infectious pancreatic necrosis Koi herpes virus Mycobacterium marinum Novirhabdovirus Pfiesteria piscicida Photobacterium damselae ssp piscicida Salmon anemia Streptococcus iniae Spring viraemia of carp Taura syndrome UDN VHS White spot Yellowhead Parasites Abergasilus Amoebic gill disease Anisakis Carp lice Ceratomyxa shasta Clinostomum marginatum Dactylogyrus vastator Diphyllobothrium Cymothoa exigua Eustrongylidosis Epizootic ulcerative syndrome Flukes Glugea Gyrodactylus salaris Henneguya zschokkei Ich (freshwater) Ich (marine) Kudoa thyrsites Lernaeocera branchialis Microsporidia Monogenea Myxobolus cerebralis Myxosporea Nanophyetus salmincola Pseudorhabdosynochus spp.
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Sign Of Hertoghe
Wikipedia
S2CID 207200169 . v t e Thyroid disease Hypothyroidism Iodine deficiency Cretinism Congenital hypothyroidism Myxedema Myxedema coma Euthyroid sick syndrome Signs and symptoms Queen Anne's sign Woltman sign Thyroid dyshormonogenesis Pickardt syndrome Hyperthyroidism Hyperthyroxinemia Thyroid hormone resistance Familial dysalbuminemic hyperthyroxinemia Hashitoxicosis Thyrotoxicosis factitia Thyroid storm Graves' disease Signs and symptoms Abadie's sign of exophthalmic goiter Boston's sign Dalrymple's sign Stellwag's sign lid lag Griffith's sign Möbius sign Pretibial myxedema Graves' ophthalmopathy Thyroiditis Acute infectious Subacute De Quervain's Subacute lymphocytic Palpation Autoimmune /chronic Hashimoto's Postpartum Riedel's Enlargement Goitre Endemic goitre Toxic nodular goitre Toxic multinodular goiter Thyroid nodule Colloid nodule
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Atrophoderma
Wikipedia
Dermatologic terminology Atrophoderma refers to conditions involving skin atrophy. [1] Types include: Follicular atrophoderma Linear atrophoderma of Moulin Atrophoderma of Pasini and Pierini References [ edit ] ^ " Atrophoderma " at Dorland's Medical Dictionary v t e Cutaneous keratosis, ulcer, atrophy, and necrobiosis Epidermal thickening keratoderma : Keratoderma climactericum Paraneoplastic keratoderma Acrokeratosis paraneoplastica of Bazex Aquagenic keratoderma Drug-induced keratoderma psoriasis Keratoderma blennorrhagicum keratosis : Seborrheic keratosis Clonal seborrheic keratosis Common seborrheic keratosis Irritated seborrheic keratosis Seborrheic keratosis with squamous atypia Reticulated seborrheic keratosis Dermatosis papulosa nigra Keratosis punctata of the palmar creases other hyperkeratosis : Acanthosis nigricans Confluent and reticulated papillomatosis Callus Ichthyosis acquisita Arsenical keratosis Chronic scar keratosis Hyperkeratosis lenticularis perstans Hydrocarbon keratosis Hyperkeratosis of the nipple and areola Inverted follicular keratosis Lichenoid keratosis Multiple minute digitate hyperkeratosis PUVA keratosis Reactional keratosis Stucco keratosis Thermal keratosis Viral keratosis Warty dyskeratoma Waxy keratosis of childhood other hypertrophy: Keloid Hypertrophic scar Cutis verticis gyrata Necrobiosis / granuloma Necrobiotic/palisading Granuloma annulare Perforating Generalized Subcutaneous Granuloma annulare in HIV disease Localized granuloma annulare Patch-type granuloma annulare Necrobiosis lipoidica Annular elastolytic giant-cell granuloma Granuloma multiforme Necrobiotic xanthogranuloma Palisaded neutrophilic and granulomatous dermatitis Rheumatoid nodulosis Interstitial granulomatous dermatitis / Interstitial granulomatous drug reaction Foreign body granuloma Beryllium granuloma Mercury granuloma Silica granuloma Silicone granuloma Zirconium granuloma Soot tattoo Tattoo Carbon stain Other/ungrouped eosinophilic dermatosis Granuloma faciale Dermis / localized CTD Cutaneous lupus erythematosus chronic: Discoid Panniculitis subacute : Neonatal ungrouped: Chilblain Lupus erythematosus–lichen planus overlap syndrome Tumid Verrucous Rowell's syndrome Scleroderma / Morphea Localized scleroderma Localized morphea Morphea–lichen sclerosus et atrophicus overlap Generalized morphea Atrophoderma of Pasini and Pierini Pansclerotic morphea Morphea profunda Linear scleroderma Atrophic / atrophoderma Lichen sclerosus Anetoderma Schweninger–Buzzi anetoderma Jadassohn–Pellizzari anetoderma Atrophoderma of Pasini and Pierini Acrodermatitis chronica atrophicans Semicircular lipoatrophy Follicular atrophoderma Linear atrophoderma of Moulin Perforating Kyrle disease Reactive perforating collagenosis Elastosis perforans serpiginosa Perforating folliculitis Acquired perforating dermatosis Skin ulcer Pyoderma gangrenosum Other Calcinosis cutis Sclerodactyly Poikiloderma vasculare atrophicans Ainhum / Pseudo-ainhum This cutaneous condition article is a stub .FERMT1, ZMPSTE24, TFAP2A, HCCS, TINF2, ERCC4, ERCC5, ERCC6, SOX18, RTEL1, PARN, XPC, XPA, NDUFB11, MMP1, TP63, KRT5, KRT14, LMNA, RECQL4, ERCC2, ERCC3, COL7A1, PORCN, TERC, TERT, POLH, POLD1, TWIST2, PLEC, ACD, MGP, COX7B, DDB2, DHCR24, DKC1, TP53, TGFB1, FKBP5, FKBP4, MEN1, TSHR, PROM1, BTG2, TIA1, SMN2, TNF, ABCA4, FST, WNK1, GUSBP1, GUSBP3, MIR381, MIR135B, RBM45, FBXO32, ADGRV1, PGPEP1, GUSBP14, DDIT4, NME8, GMNN, SFRP2, ARIH1, KLK8, RASSF1, SMN1, PGR, ATXN1, CD44, GPI, GAST, FSHMD1A, ELN, CELSR3, ACE, DCN, COL17A1, CAT, HTT, C2, BMP4, BGN, BCL2, AQP5, APOE, APOC1, AEBP1, NR3C1, HIF1A, S100A8, NEFH, RPGR, RET, PIK3CG, PIK3CD, PIK3CB, PIK3CA, ACTB, PGC, NEFM, HLA-DRB1, NEDD4, NR3C2, ATXN3, LTA, TNFRSF9, IL6, IL1RN, IGF1, DUX4
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Craniomandibular Osteopathy
Wikipedia
A similar disease seen in young Bullmastiffs is known as calvarial hyperostotic syndrome . It is also similar to human infantile cortical hyperostosis . ... Retrieved 2006-08-26 . ^ McConnell J, Hayes A, Platt S, Smith K (2006). "Calvarial hyperostosis syndrome in two bullmastiffs". Vet Radiol Ultrasound . 47 (1): 72–7. doi : 10.1111/j.1740-8261.2005.00108.x .
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Short-Chain Acyl-Coa Dehydrogenase Deficiency
Medlineplus
This disorder is sometimes mistaken for Reye syndrome, a severe condition that may develop in children while they appear to be recovering from viral infections such as chicken pox or flu. Most cases of Reye syndrome are associated with the use of aspirin during these viral infections.
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Radioulnar Synostosis
Wikipedia
Radioulnar synostosis Other names Radioulnar fusion Congenital radioulnar synostosis in a 7 year old boy Specialty Orthopaedics Radioulnar synostosis is a rare condition where there is an abnormal connection between the radius and ulna bones of the forearm. [1] This can be present at birth (congenital), when it is a result of a failure of the bones to form separately, or following an injury (post-traumatic). [2] It typically causes restricted movement of the forearm, in particular rotation ( pronation and supination ), though is not usually painful unless it causes subluxation of the radial head . [1] It can be associated with dislocation of the radial head which leads to limited elbow extension. [2] Contents 1 Types 1.1 Congenital 1.2 Acquired 2 Treatment 3 References 4 External links Types [ edit ] Congenital [ edit ] Congenital radioulnar synostosis is rare, with approximately 350 cases reported in journals, and it typically affects both sides (bilateral) and can be associated with other skeletal problems such as hip and knee abnormalities, finger abnormalities ( syndactyly or clinodactyly ), or Madelung's deformity . [1] It is sometimes part of known genetic syndromes such as Klinefelter syndrome (48,XXXY variant), Apert , Williams , Cornelia de Lange , or Holt-Oram . [1] [3] It has been reported to run in families typically following an autosomal dominant inheritance pattern which means children of an affected parent have a 50% chance of having the condition. [3] When associated with amegakaryocytic thrombocytopenia this inheritance has been found to be caused by mutations to the HOXA11 gene. [4] Acquired [ edit ] Post-traumatic cases are most likely to develop following surgery for a forearm fracture , this is more common with high-energy injuries where the bones are broken into many pieces ( comminuted ). [1] It can also develop following soft tissue injury to the forearm where there is haematoma formation. [ citation needed ] Treatment [ edit ] It is sometimes possible to correct the problem with surgery, though this has high failure rates for treatment of post-traumatic radioulnar synostosis. [1] Indication for the surgical treatment of congenital radioulnar synostosis include severe disability due to bilateral disorder or hyperpronation ≥90 [1] References [ edit ] ^ a b c d e f Wurapa, Raymond (7 January 2017).
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Swan Neck Deformity
Wikipedia
It is commonly caused by injury or inflammatory conditions like rheumatoid arthritis or sometimes familial (congenital, like Ehlers–Danlos syndrome [1] ). Contents 1 Pathophysiology 2 Diagnosis 3 Treatment 4 References 5 External links Pathophysiology [ edit ] Swan neck deformity has many of possible causes arising from the DIP, PIP , or even the MCP joints. ... "Dynamic Swan Neck Deformity in a Patient with Ehlers–Danlos Syndrome" . The Journal of Hand Surgery .
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Very Long-Chain Acyl-Coa Dehydrogenase Deficiency
Medlineplus
In affected children, this disorder is sometimes mistaken for Reye syndrome, a severe disorder that may develop in children while they appear to be recovering from viral infections such as chicken pox or flu. Most cases of Reye syndrome are associated with the use of aspirin during these viral infections.
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Papillary Renal Cell Carcinoma
Orphanet
It is typically multifocal, bilateral, and in most cases sporadic, although different hereditary syndromes, such as Hereditary leiomyoma renal cell carcinoma, Birt-Hogg-Dubé syndrome and Tuberous sclerosis, may predispose to the development of papillary renal cell carcinoma.MET, MITF, PRCC, VHL, TFE3, KRT7, ERBB2, GSTP1, SLC2A1, ELOC, POMC, PIK3CA, ADIPOQ, RPL14, INPP4B, FPGT, TNFSF10, CRADD, UNC5C, TAGLN2, BAP1, KDM5C, PEBP1, MLLT10, PAK1, TSC1, TP53, TGM2, PDHB, HNF1B, HNF1A, NF2, SOD2, SLC5A3, PGK1, ACY1, RYR1, RELA, PVALB, PTGS2, PTEN, ZNF536, ACHE, KEAP1, AHNAK, LMAN2L, CARD11, SLC49A4, NAV3, ZNF765, NLRP12, ZNF804A, CSMD3, LRRK2, ASB15, DNHD1, FAAH2, FLCN, OR4C13, VMO1, MSGN1, FAM111B, BIRC7, SPTBN4, CUL7, FMN2, NDRG1, CPQ, BTG3, AKAP13, RNF139, PDXDC1, SYNE2, PRAME, YIPF3, PNKD, SETD2, SHANK1, LRP1B, TET2, PBRM1, PIDD1, AP5M1, OGG1, SFRP2, APRT, MUC4, IL6, ALDH1A1, ALK, ALOX5, IFNA2, HSPD1, HSPB1, HSPA9, ALOX12B, ANXA4, APAF1, BIRC5, HARS1, EEF2, BCHE, GSTT1, GSTM1, GRB7, GJB1, EPAS1, MTOR, IL6R, IL4R, IL13, KRT32, CNN2, SCARB1, CASP2, CAPG, M6PR, ALAD, LDHB, L1CAM, CRABP1, KRT8, KCNMA1, DAPK1, CTSD, CTSB, CRYAB, FLT1, CDC73, HABP2, LMNA, FOXE1, MINPP1, VEGFA, AMACR, KDR, CD38, FH, MME, RASSF1, CA9, MYC, KIT, SNORD14D, SNORD14C, CD47, MIR1180, TWSG1, MIR1293, MIR379, KMT2C, ACE2, FBXO47, EIF2AK4, MIR34A, MIR200C, MIR181C, MIR134, MIR127, FBXO11, AKT1, DDR1, RAB37, APC, CDC34, SETDB2, BRAF, SNORD35B, RIOX2, BSG, BUB1, SNORD14E, SNORD14B, MEG3, DHCR24, LARP6, CDH1, HIF1A, TOP2A, TIMP3, TIMP1, UBE2K, SYP, IGFBP7, SLC16A1, SFPQ, RRM2, SNORD15A, CD82, PYCR1, PTK7, CFP, PAX2, MUC1, TBC1D25, OAT, NONO, NFE2L2, XRCC1, PAX8, FZD1, KDM4C, CDR2, CMA1, APH1A, CD274, CLDN7, MCTS1, MCAT, UBE2S, HAVCR1, ACE, CUL3, RALBP1, EGF, EGFR, ELAVL2, ETFA, NAPSA, FGFR2, FOLH1, GABPA, MIR3199-2
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Dpm3-Cdg
Orphanet
DPM3-CDG is an extremely rare form of CDG syndrome (see this term) characterized clinically in the single reported case by muscle weakness, waddling gait and dilated cardiomyopathy (see this term).
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Histoplasmosis
Wikipedia
Severe infections can cause hepatosplenomegaly , lymphadenopathy , and adrenal enlargement. [3] Lesions have a tendency to calcify as they heal. Presumed ocular histoplasmosis syndrome causes chorioretinitis , where the choroid and retina of the eyes are scarred, resulting in a loss of vision not unlike macular degeneration . ... These include recurrent pneumonia, respiratory failure , fibrosing mediastinitis , superior vena cava syndrome , pulmonary vessel obstruction, and progressive fibrosis of lymph nodes. ... "Intravitreal anti-vascular endothelial growth factor therapy for choroidal neovascularization secondary to ocular histoplasmosis syndrome". Retina . 32 (3): 468–72. doi : 10.1097/IAE.0b013e318229b220 . ... "Disseminated bilateral chorioretinitis due to Histoplasma capsulatum in a patient with the acquired immunodeficiency syndrome". Ophthalmology . 92 (8): 1159–64. doi : 10.1016/s0161-6420(85)33921-0 . ... "Cutaneous histoplasmosis in patients with acquired immunodeficiency syndrome". Cutis . 72 (6): 439–45. PMID 14700213 . ^ James WD, Berger TG, et al. (2006).
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Recurrent Miscarriage
Wikipedia
After three or more losses, a thorough evaluation is recommended by American Society of Reproductive Medicine . [2] About 1% of couples trying to have children are affected by recurrent miscarriage. [3] [4] Contents 1 Causes 1.1 Chromosomal disorders 1.2 Lifestyle factors 1.3 Anatomical conditions 1.3.1 Cervical conditions 1.4 Endocrine disorders 1.5 Thrombophilia 1.6 Immune factors 1.6.1 Antiphospholipid syndrome 1.6.2 Thyroid antibodies 1.6.3 Increased uterine NK cells 1.6.4 Parental HLA sharing 1.6.5 Male-specific minor histocompatibility 1.7 Ovarian factors 1.7.1 Luteal phase defect 1.8 Infection 2 Assessment 3 Treatment 4 Psychological effects of miscarriages 5 Association with later disease 6 References 7 Bibliography 8 External links Causes [ edit ] Relative incidences of causative findings in cases with recurrent miscarriage. [5] There are various causes for recurrent miscarriage, and some can be treated. ... Unrecognized or poorly treated diabetes mellitus leads to increased miscarriages. Women with polycystic ovary syndrome also have higher loss rates possibly related to hyperinsulinemia or excess androgens. ... Thrombophilia may explain up to 49–65% of recurrent miscarriages. [18] Immune factors [ edit ] A common feature of immune factors in causing recurrent pregnancy loss appears to be a decreased maternal immune tolerance towards the fetus. [19] Antiphospholipid syndrome [ edit ] The antiphospholipid syndrome is an autoimmune disease that is a common cause of recurrent pregnancy loss. [4] [8] Around 15% of the women who have recurrent miscarriages have high levels of antiphospholipid antibodies. [4] Women who have had more than one miscarriage in the first trimester, or a miscarriage in the second trimester, may have their blood tested for antibodies, to determine if they have antiphospholipid syndrome. [4] Women diagnosed with antiphospholipid syndrome generally take aspirin or heparin in subsequent pregnancies, but questions remain due to the lack of high quality trials. [20] [21] Thyroid antibodies [ edit ] Anti-thyroid autoantibodies are associated with an increased risk of recurrent miscarriage with an odds ratio of 2.3 with a 95% confidence interval of 1.5–3.5. [22] Increased uterine NK cells [ edit ] Natural killer cells , a type of white blood cell, are present in uterine tissue. ... In pregnant women with a history of recurrent miscarriage, anticoagulants seem to increase the live birth rate among those with antiphospholipid syndrome and perhaps those with congenital thrombophilia but not in those with unexplained recurrent miscarriage. [28] One study found that in many women with chronic endometritis, "fertility was restored after appropriate antibiotic treatment." [26] There are currently no treatments for women with unexplained recurrent pregnancy loss. ... External links [ edit ] Classification D ICD - 10 : N96 ICD - 9-CM : 629.81 MeSH : D000026 External resources eMedicine : article/260495 Frequently Asked Questions About Recurrent Pregnancy Loss v t e Reproductive health Rights Compulsory sterilization Contraceptive security Genital integrity Circumcision controversies Genital modification and mutilation Intersex Education Genetic counseling Pre-conception counseling Sex education Planning Assisted reproductive technology Birth control Childfree / Childlessness Parenting Adoption Childbirth Foster care Safe sex Health Men's Women's Vulvovaginal Research Self-report sexual risk behaviors Pregnancy Abortion Birth spacing Maternal health Obstetrics Options counseling Pregnancy from rape Pregnant patients' rights Prenatal care Teenage pregnancy Preteen pregnancy Unintended pregnancy Medicine Andrology Genitourinary medicine Gynaecology Obstetrics and gynaecology Reproductive endocrinology and infertility Sexual medicine Disorder Disorders of sex development Infertility Reproductive system disease Sexual dysfunction Sexually transmitted infection Clinic By country China India Iran Ireland Pakistan Philippines Singapore United Kingdom Teen United States Teen pregnancy Birth control History Birth control movement in the United States History of condoms Social hygiene movement Timeline of reproductive rights legislation Policy One-child policy Two-child policy Financial Baby bonus Bachelor tax Child benefit Tax on childlessness v t e Female diseases of the pelvis and genitals Internal Adnexa Ovary Endometriosis of ovary Female infertility Anovulation Poor ovarian reserve Mittelschmerz Oophoritis Ovarian apoplexy Ovarian cyst Corpus luteum cyst Follicular cyst of ovary Theca lutein cyst Ovarian hyperstimulation syndrome Ovarian torsion Fallopian tube Female infertility Fallopian tube obstruction Hematosalpinx Hydrosalpinx Salpingitis Uterus Endometrium Asherman's syndrome Dysfunctional uterine bleeding Endometrial hyperplasia Endometrial polyp Endometriosis Endometritis Menstruation Flow Amenorrhoea Hypomenorrhea Oligomenorrhea Pain Dysmenorrhea PMS Timing Menometrorrhagia Menorrhagia Metrorrhagia Female infertility Recurrent miscarriage Myometrium Adenomyosis Parametrium Parametritis Cervix Cervical dysplasia Cervical incompetence Cervical polyp Cervicitis Female infertility Cervical stenosis Nabothian cyst General Hematometra / Pyometra Retroverted uterus Vagina Hematocolpos / Hydrocolpos Leukorrhea / Vaginal discharge Vaginitis Atrophic vaginitis Bacterial vaginosis Candidal vulvovaginitis Hydrocolpos Sexual dysfunction Dyspareunia Hypoactive sexual desire disorder Sexual arousal disorder Vaginismus Urogenital fistulas Ureterovaginal Vesicovaginal Obstetric fistula Rectovaginal fistula Prolapse Cystocele Enterocele Rectocele Sigmoidocele Urethrocele Vaginal bleeding Postcoital bleeding Other / general Pelvic congestion syndrome Pelvic inflammatory disease External Vulva Bartholin's cyst Kraurosis vulvae Vestibular papillomatosis Vulvitis Vulvodynia Clitoral hood or clitoris Persistent genital arousal disorder Authority control NDL : 01106844
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Central Nervous System Fatigue
Wikipedia
It is important to avoid hyperthermia and dehydration , as they are detrimental to athletic performance and can be fatal. [27] Chronic fatigue syndrome [ edit ] Chronic fatigue syndrome is a name for a group of diseases that are dominated by persistent fatigue. ... J Athl Train. 1996;31(3):248–252. ^ Evangard B; Schacterie R.S.; Komaroff A. L. (1999). "Chronic fatigue syndrome: new insights and old ignorance" . ... Central basis of muscle fatigue in chronic fatigue syndrome. Neurology 43:125–131, 1993 ^ Riley, M. ... Aerobic work capacity in patients with chronic fatigue syndrome. Br. Med. J. 301:953–956, 1990 ^ Stokes, M. ... Normal muscle strength and fatigability in patients with effort syndromes. Br. Med. J. 297:1014–1017, 1988.
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Delusional Disorder
Wikipedia
External links [ edit ] Classification D ICD - 10 : F22.0 ICD - 9-CM : 297.1 MeSH : D010259 External resources eMedicine : article/292991 Media related to Delusional disorders at Wikimedia Commons v t e Mental and behavioral disorders Adult personality and behavior Gender dysphoria Ego-dystonic sexual orientation Paraphilia Fetishism Voyeurism Sexual maturation disorder Sexual relationship disorder Other Factitious disorder Munchausen syndrome Intermittent explosive disorder Dermatillomania Kleptomania Pyromania Trichotillomania Personality disorder Childhood and learning Emotional and behavioral ADHD Conduct disorder ODD Emotional and behavioral disorders Separation anxiety disorder Movement disorders Stereotypic Social functioning DAD RAD Selective mutism Speech Stuttering Cluttering Tic disorder Tourette syndrome Intellectual disability X-linked intellectual disability Lujan–Fryns syndrome Psychological development ( developmental disabilities ) Pervasive Specific Mood (affective) Bipolar Bipolar I Bipolar II Bipolar NOS Cyclothymia Depression Atypical depression Dysthymia Major depressive disorder Melancholic depression Seasonal affective disorder Mania Neurological and symptomatic Autism spectrum Autism Asperger syndrome High-functioning autism PDD-NOS Savant syndrome Dementia AIDS dementia complex Alzheimer's disease Creutzfeldt–Jakob disease Frontotemporal dementia Huntington's disease Mild cognitive impairment Parkinson's disease Pick's disease Sundowning Vascular dementia Wandering Other Delirium Organic brain syndrome Post-concussion syndrome Neurotic , stress -related and somatoform Adjustment Adjustment disorder with depressed mood Anxiety Phobia Agoraphobia Social anxiety Social phobia Anthropophobia Specific social phobia Specific phobia Claustrophobia Other Generalized anxiety disorder OCD Panic attack Panic disorder Stress Acute stress reaction PTSD Dissociative Depersonalization disorder Dissociative identity disorder Fugue state Psychogenic amnesia Somatic symptom Body dysmorphic disorder Conversion disorder Ganser syndrome Globus pharyngis Psychogenic non-epileptic seizures False pregnancy Hypochondriasis Mass psychogenic illness Nosophobia Psychogenic pain Somatization disorder Physiological and physical behavior Eating Anorexia nervosa Bulimia nervosa Rumination syndrome Other specified feeding or eating disorder Nonorganic sleep Hypersomnia Insomnia Parasomnia Night terror Nightmare REM sleep behavior disorder Postnatal Postpartum depression Postpartum psychosis Sexual dysfunction Arousal Erectile dysfunction Female sexual arousal disorder Desire Hypersexuality Hypoactive sexual desire disorder Orgasm Anorgasmia Delayed ejaculation Premature ejaculation Sexual anhedonia Pain Nonorganic dyspareunia Nonorganic vaginismus Psychoactive substances, substance abuse and substance-related Drug overdose Intoxication Physical dependence Rebound effect Stimulant psychosis Substance dependence Withdrawal Schizophrenia , schizotypal and delusional Delusional Delusional disorder Folie à deux Psychosis and schizophrenia-like Brief reactive psychosis Schizoaffective disorder Schizophreniform disorder Schizophrenia Childhood schizophrenia Disorganized (hebephrenic) schizophrenia Paranoid schizophrenia Pseudoneurotic schizophrenia Simple-type schizophrenia Other Catatonia Symptoms and uncategorized Impulse control disorder Klüver–Bucy syndrome Psychomotor agitation Stereotypy
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Vaccine Adverse Event
Wikipedia
Current scientific evidence does not support claims of vaccines causing various disorders. [10] [11] The debate is complicated by misconceptions around the recording and reporting of adverse events by anti-vaccination activists. [12] According to authorities, anti-vaccination websites greatly exaggerate the risk of serious adverse effects from vaccines and falsely describe conditions such as autism and shaken baby syndrome as vaccine injuries, [13] [14] [15] leading to misconceptions about the safety and effectiveness of vaccines. [16] [17] This has had the result of stigmatizing autistic people and the parents who had them immunized. [18] The oral polio vaccine (OPV) is unusual in that it contains a live attenuated virus that can be excreted leading, in under-vaccinated communities, to secondary infection. [19] Since 2000, more than 10 billion doses of OPV have been administered to nearly 3 billion children worldwide. ... The program's success in tracking vaccine injuries has been questioned by some, who allege medical practitioners frequently fail to make reports. [34] Others say that it may overstate possible injuries since many neurological problems in childhood may manifest around the same ages when vaccines are routinely administered. [ citation needed ] Dravet syndrome is one example of a genetically based neurological disease which frequently manifests at the time of childhood vaccinations. [35] Vaccine Safety Datalink [ edit ] The Vaccine Safety Datalink (VSD), funded by the Centers for Disease Control , is composed of databases from several organizations containing information regarding health outcomes for millions of US citizens and to enhance assessment of vaccine injuries. ... "The antivaccine lie that just won't die: The claim that shaken baby syndrome is really due to "vaccine injury " " . ... PMID 7503351 . ^ https://www.dravetfoundation.org/what-is-dravet-syndrome/ ^ "£3.5m paid out in vaccine damages" . ... Secretary of Health and Human Services Alternative vaccination schedule Related Epidemiology Eradication of infectious diseases Every Child by Two List of vaccine topics # WHO-EM ‡ Withdrawn from market Clinical trials : † Phase III § Never to phase III v t e Adverse drug reactions Antibiotics Penicillin drug reaction Sulfonamide hypersensitivity syndrome Urticarial erythema multiforme Adverse effects of fluoroquinolones Red man syndrome Jarisch–Herxheimer reaction Hormones Steroid acne Steroid folliculitis Chemotherapy Chemotherapy-induced acral erythema Chemotherapy-induced hyperpigmentation Scleroderma-like reaction to taxanes Hydroxyurea dermopathy Exudative hyponychial dermatitis Anticoagulants Anticoagulant-induced skin necrosis Warfarin necrosis Vitamin K reaction Texier's disease Immunologics Adverse reaction to biologic agents Leukotriene receptor antagonist-associated Churg–Strauss syndrome Methotrexate-induced papular eruption Adverse reaction to cytokines Other drugs Anticonvulsant hypersensitivity syndrome Allopurinol hypersensitivity syndrome Vaccine adverse event Eczema vaccinatum Bromoderma Halogenoderma Iododerma General Skin and body membranes Acute generalized exanthematous pustulosis Bullous drug reaction Drug-induced acne Drug-induced angioedema Drug-related gingival hyperplasia Drug-induced lichenoid reaction Drug-induced lupus erythematosus Drug-induced nail changes Drug-induced pigmentation Drug-induced urticaria Stevens–Johnson syndrome Injection site reaction Linear IgA bullous dermatosis Toxic epidermal necrolysis HIV disease-related drug reaction Photosensitive drug reaction Other Drug-induced pseudolymphoma Fixed drug reaction Serum sickness-like reaction
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Mixed Connective Tissue Disease
Wikipedia
Mixed connective tissue disease Other names Sharp's syndrome [1] Specialty Immunology , rheumatology Differential diagnosis CPT2 . ... In some studies these patients become reclassified over time with other diseases, such as rheumatoid arthritis in 9%, SLE in 15%, and scleroderma in 21% of cases. [27] Such progression is, in part, determined genetically, thus SLE is more likely in patients with HLA-DR3 and scleroderma in patients with HLA-DR5. [24] Epidemiology [ edit ] The prevalence of MCTD is higher than that of dermatomyositis and lower than that of SLE. [28] In a 2011 Norwegian study, the prevalence of MCTD was 3.8 per 100,000 adults, with an incidence of 2.1 per million per year. [29] MCTD is much more frequent in women than in men at between a 3:1 to 16:1 ratio, and in women younger than 50. [10] The general age at onset is around 15–25 years old. [ citation needed ] See also [ edit ] Autoimmunity Overlap syndrome Rheumatoid arthritis Autoimmune disease Scleroderma Systemic lupus erythematosus Polymyositis Rheumatology References [ edit ] ^ a b Rapini RP, Bolognia JL, Jorizzo JL (2007). ... "Mixed connective tissue disease--an apparently distinct rheumatic disease syndrome associated with a specific antibody to an extractable nuclear antigen (ENA)". ... "Undifferentiated connective tissue syndromes" . Arthritis and Rheumatism . 23 (3): 341–3. doi : 10.1002/art.1780230312 . ... External links [ edit ] Classification D ICD - 10 : M35.1 ICD - 9-CM : 710.8 MeSH : D008947 DiseasesDB : 8312 External resources eMedicine : med/3417 Patient UK : Mixed connective tissue disease Orphanet : 809 v t e Systemic connective tissue disorders General Systemic lupus erythematosus Drug-induced SLE Libman–Sacks endocarditis Inflammatory myopathy Myositis Dermatopolymyositis Dermatomyositis / Juvenile dermatomyositis Polymyositis * Inclusion body myositis Scleroderma Systemic scleroderma Progressive systemic sclerosis CREST syndrome Overlap syndrome / Mixed connective tissue disease Other hypersensitivity / autoimmune Sjögren syndrome Other Behçet's disease Polymyalgia rheumatica Eosinophilic fasciitis Eosinophilia–myalgia syndrome fibrillin Marfan syndrome Congenital contractural arachnodactylyRNPC3, LSM2, HLA-DRB1, SNRNP70, HLA-DRB4, RBM45, TRBV20OR9-2, FSCN1, SNRPA, HNRNPDL, RO60, TRB, TNF, SFTPD, TNFRSF1A, CDR3, PIK3R3, CD40LG, CDK2AP2, SUB1, PTBP1, BTG3, RPP14, POLG2, LAMTOR2, SF3B6, ENAH, NT5C1A, IL17F, H3P44, S100A9, PON1, PSMD12, HNRNPAB, COL17A1, CRP, DSG3, ERG, F8, FOS, CBLIF, HLA-DOA, HLA-DPB1, HLA-DQA1, HLA-DQB1, HLA-DRB3, HNRNPC, CDKN2A, IFNA1, IFNA13, IL2RA, IL6, IL10, IL12B, IL17A, IRF7, MPP1, MUC1, NCAM1, P4HB, H3P8