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Parastremmatic Dwarfism
Orphanet
Clinical description Radiographs show bowing of long bones, platyspondyly and a very rough, irregular metaphyseal and epiphyseal bone texture. Etiology The syndrome is caused by a heterozygous mutation in the TRPV4 gene (12q24.1).
- Abducens Palsy Omim
- Adult-Onset Autosomal Recessive Sideroblastic Anemia Orphanet
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Stretch Marks
Mayo_clinic
This can result from corticosteroid medicine use or a disease such as Cushing syndrome. When to see a doctor See your health care provider if you're concerned about the appearance of your skin or if the stretch marks cover large areas of your body. ... Risk factors Anyone can develop stretch marks, but some factors increase your likelihood of getting them, including: Being female Having a personal or family history of stretch marks Being pregnant, especially if you're young Rapid growth in adolescence Rapidly gaining or losing weight Using corticosteroids Having breast enlargement surgery Exercising and using anabolic steroids Having a genetic disorder such as Cushing syndrome or Marfan syndrome Diagnosis Stretch marks don't usually need to be diagnosed.FBN1, COL5A1, AIP, PDE11A, TGFBR2, TGFBR1, ENPP1, CRH, COL5A2, GNAS, COL1A1, USP8, TP53, PRKACA, BRCA2, CUL4B, ABCC6, SH3BP2, PDE8B, SMAD3, PRKAR1A, C1QL1, ELN, GJB6, KCNQ1, ESR1, KCNJ10, GLP1R, FOS, MMP2, MMP9, GJB2, NPY, LRP2, NR3C1, FN1, TJP1, OXTR, AR, SLC31A1, SST, RXFP3, TAC3, SNCA, SOX10, EVI5, ST2, SYP, TRPV1, BSND, TBX1, VCAM1, TRBV20OR9-2, TYR, TRH, TH, TNF, ADCYAP1, CUBN, BDP1, ZGLP1, MIR205, ARSI, SLC17A8, CCDC50, RLN3, PANX3, SLC2A13, UCN3, EHMT1, TMPRSS3, MCOLN1, PANX2, MCOLN3, NRP1, ANO1, P4HTM, COQ6, PANX1, RIMBP2, CEP104, PRDX6, SLC22A2, KCNK6, DCLK1, KCNQ4, NOL3, PER2, SLC22A4, PAX3, SLC6A4, CYP19A1, GLB1, GJB1, GHR, GCG, GABRG3, GABPA, FGFR2, EGF, E2F1, DRD2, COCH, DCX, CSF1, HCRTR1, CRHR1, COL2A1, CLC, CDH13, CASP3, CALCR, CALCA, CALB2, CALB1, AVPR1A, ANK2, AIF1, GRM8, HIF1A, SLC5A3, NPY2R, SLC2A3, S100B, S100A12, POU2F2, POMC, PNOC, PGR, PCNA, PARP1, CLDN11, OPRL1, NUCB2, NFE2L2, HOXB1, MYO7A, ABCC1, MMP8, MMP3, MITF, KCNE1, ITPR3, ITPR2, ITPR1, IL10, IGF1, IDH2, LINC02210-CRHR1
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Congenital Hypotonia, Epilepsy, Developmental Delay, And Digital Anomalies
Omim
Description Congenital hypotonia, epilepsy, developmental delay, and digital anomalies (CHEDDA) is a syndromic neurodevelopmental disorder characterized by severe global developmental delay, impaired intellectual development with poor or absent language, significant motor disability with inability to walk, dysmorphic facial features, skeletal anomalies, and variable congenital anomalies. ... One of the patients (patient 8), who died at 2 months of age, had previously been reported by Mosca et al. (2007) as having a multiple congenital anomaly syndrome with dysmorphic facial features, cleft palate, axial hypotonia, peripheral hypertonia, polymicrogyria, and cerebellar vermis hypoplasia. ... ATN1 also lies within the critical region for Pallister-Killian syndrome (PKS; 601803), which has an overlapping phenotype.
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Surfactant Dysfunction
Medlineplus
The most severe form of this condition causes respiratory distress syndrome in newborns. Affected babies have extreme difficulty breathing and are unable to get enough oxygen. The lack of oxygen can damage the baby's brain and other organs. This syndrome leads to respiratory failure, and most babies with this form of the condition do not survive more than a few months. ... One type, called SP-B deficiency, causes respiratory distress syndrome in newborns. Other types, known as SP-C dysfunction and ABCA3 deficiency, have signs and symptoms that range from mild to severe.
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Hyposmia
Wikipedia
In 2012 an estimated 9.8 million people aged 40 and older in the United States had hyposmia and an additional 3.4 million had anosmia /severe hyposmia. [2] Hyposmia might be a very early sign of Parkinson's disease . [3] Hyposmia is also an early and almost universal finding in Alzheimer's disease and dementia with Lewy bodies . [3] Lifelong hyposmia could be caused by Kallmann syndrome [4] or Autistic Spectrum Disorder . [5] Along with other chemosensory disturbances, hyposmia can be a key indicator of COVID-19 . [6] [7] Epidemiology [ edit ] The National Health and Nutrition Examination Survey ( NHANES ) collected data on chemosensory function (taste and smell) in a nationally-representative sample of US civilian, non-institutionalized persons in 2012. [8] Olfactory function was assessed on persons aged 40 years and older with an 8-item, odor identification test (Pocket Smell Tests™, Sensonics, Inc., Haddon Heights, NJ). ... New York: Demos Medical Publishing. ^ Arkoncel, ML; Arkoncel, FR; Lantion-Ang, FL (March 2011). "A case of Kallmann syndrome" . BMJ Case Reports . 2011 . doi : 10.1136/bcr.01.2011.3727 . PMC 3070321 . PMID 22700069 . Kallmann syndrome (KS), a rare genetic disorder, refers to the association between hypogonadotropic hypogonadism and anosmia or hyposmia due to abnormal migration of olfactory axons and gonadotropin-releasing hormone producing neurons. ^ Tonacci, Alessandro; Billeci, Lucia; Tartarisco, Gennaro; Ruta, Liliana; Muratori, Filippo; Pioggia, Giovanni; Gangemi, Sebastiano (2 January 2017).SNCA, LRRK2, CHD7, SCN9A, GIGYF2, SEMA3A, NSMF, PROK2, GBA, FGFR1, FGF8, PROKR2, SOX10, SMCHD1, ATP13A2, SLC39A14, FLRT3, DNAJC13, PARK7, ADCY3, HTRA2, IL17RD, VPS13C, WDR11, VPS35, PINK1, CEP290, SPRY4, KISS1R, CCDC141, IFT27, TSHZ1, PTPN11, SCP2, COL4A2, DCC, DUSP6, EIF4G1, ANOS1, PRKN, PODXL, DNAJC6, FEZF1, HS6ST1, TACR3, UCHL1, FGF17, HESX1, SLC6A3, SIT1, OBP2A, SEMA7A, C9orf72, DUSP26, ACKR1, GNAL, GNRH1, SST, RMRP, CNGB1
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Stomatin-Deficient Cryohydrocytosis With Neurologic Defects
Omim
The disorder combines the neurologic features of Glut1 deficiency syndrome-1 (GLUT1DS1; 606777), resulting from impaired glucose transport at the blood-brain barrier, and hemolytic anemia/pseudohyperkalemia with stomatocytosis, resulting from a cation leak in erythrocytes (summary by Bawazir et al., 2012). ... Both of the stomatin-deficient patients showed a neurologic syndrome of seizures, mental retardation, and cataracts associated with hepatosplenomegaly, a combination that had not previously been described. ... Like patient D-II-2, she presented with a predominantly neurologic syndrome of seizures, spastic paraplegia, mental retardation, and cataracts associated with massive hepatosplenomegaly and 'blueberry muffin' spots on the skin.
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Congenital Disorder Of Glycosylation, Type Ig
Omim
Description Congenital disorders of glycosylation (CDG), previously called carbohydrate-deficient glycoprotein syndromes (CDGSs), are a group of hereditary multisystem disorders first recognized by Jaeken et al. (1980). ... Kranz et al. (2007) noted similarities between this phenotype and Roifman syndrome (300258), and suggested that some cases of Roifman syndrome may be congenital disorders of glycosylation.
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Striatonigral Degeneration, Infantile
Omim
Many features of BSN overlap with Leigh syndrome (256000) and certain metabolic disorders, including glutaric acidemia I (231670) and methylmalonic aciduria (251000). See also Aicardi-Goutieres syndrome (225750) (Mito et al., 1986; De Meirleir et al., 1995). ... Inheritance Straussberg et al. (2002) pointed out that IBSN encompasses several syndromes of bilateral symmetric, spongy degeneration of the caudate nucleus, putamen, and globus pallidus.
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Heart Block, Congenital
Omim
Cannom and Hancock (1974) described a distinctive syndrome of cardiomyopathy, probably congenital, with mitral regurgitation, complete heart block, and atrial arrhythmia in 4 unrelated male patients. ... In the mother, features of both SLE and Sjogren syndrome (270150) developed 26 years after the birth of her son. ... Manthorpe and Manthorpe (1992) found 4 children with congenital complete heart block among the offspring of 91 Swedish mothers and 71 Danish mothers with primary Sjogren syndrome--a relative risk of about 500, making the incidence of congenital heart block in the general population to be 1 per 20,000.
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Microcystic Adnexal Carcinoma
Wikipedia
Retrieved 4 December 2020 . v t e Cancers of skin and associated structures Glands Sweat gland Eccrine Papillary eccrine adenoma Eccrine carcinoma Eccrine nevus Syringofibroadenoma Spiradenoma Apocrine Cylindroma Dermal cylindroma Syringocystadenoma papilliferum Papillary hidradenoma Hidrocystoma Apocrine gland carcinoma Apocrine nevus Eccrine / apocrine Syringoma Hidradenoma or Acrospiroma / Hidradenocarcinoma Ceruminous adenoma Sebaceous gland Nevus sebaceous Muir–Torre syndrome Sebaceous carcinoma Sebaceous adenoma Sebaceoma Sebaceous nevus syndrome Sebaceous hyperplasia Mantleoma Hair Pilomatricoma / Malignant pilomatricoma Trichoepithelioma Multiple familial trichoepithelioma Solitary trichoepithelioma Desmoplastic trichoepithelioma Generalized trichoepithelioma Trichodiscoma Trichoblastoma Fibrofolliculoma Trichilemmoma Trichilemmal carcinoma Proliferating trichilemmal cyst Giant solitary trichoepithelioma Trichoadenoma Trichofolliculoma Dilated pore Isthmicoma Fibrofolliculoma Perifollicular fibroma Birt–Hogg–Dubé syndrome Hamartoma Basaloid follicular hamartoma Folliculosebaceous cystic hamartoma Folliculosebaceous-apocrine hamartoma Nails Neoplasms of the nailbed This Epidermal nevi, neoplasms, cysts article is a stub .
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Sertoli Cell Tumour
Wikipedia
See also [ edit ] Androgen-dependent syndromes Leydig cell tumour Sertoli-Leydig cell tumour Sertoli cell nodule Notes [ edit ] ^ Young, Robert H. (2005-01-01). ... PMID 19037884 . ^ Vegter AR, Kooistra HS, van Sluijs FJ, van Bruggen LW, Ijzer J, Zijlstra C, Okkens AC (October 2008). "Persistent Mullerian Duct Syndrome in a Miniature Schnauzer Dog with Signs of Feminization and a Sertoli Cell Tumour". ... External links [ edit ] Media related to Sertoli cell tumor at Wikimedia Commons Classification D ICD - 9-CM : 183.0 , 256.1 ICD-O : 8631 MeSH : D012707 v t e Tumors of the female urogenital system Adnexa Ovaries Glandular and epithelial / surface epithelial- stromal tumor CMS: Ovarian serous cystadenoma Mucinous cystadenoma Cystadenocarcinoma Papillary serous cystadenocarcinoma Krukenberg tumor Endometrioid tumor Clear-cell ovarian carcinoma Brenner tumour Sex cord–gonadal stromal Leydig cell tumour Sertoli cell tumour Sertoli–Leydig cell tumour Thecoma Granulosa cell tumour Luteoma Sex cord tumour with annular tubules Germ cell Dysgerminoma Nongerminomatous Embryonal carcinoma Endodermal sinus tumor Gonadoblastoma Teratoma / Struma ovarii Choriocarcinoma Fibroma Meigs' syndrome Fallopian tube Adenomatoid tumor Uterus Myometrium Uterine fibroids/leiomyoma Leiomyosarcoma Adenomyoma Endometrium Endometrioid tumor Uterine papillary serous carcinoma Endometrial intraepithelial neoplasia Uterine clear-cell carcinoma Cervix Cervical intraepithelial neoplasia Clear-cell carcinoma SCC Glassy cell carcinoma Villoglandular adenocarcinoma Placenta Choriocarcinoma Gestational trophoblastic disease General Uterine sarcoma Mixed Müllerian tumor Vagina Squamous-cell carcinoma of the vagina Botryoid rhabdomyosarcoma Clear-cell adenocarcinoma of the vagina Vaginal intraepithelial neoplasia Vaginal cysts Vulva SCC Melanoma Papillary hidradenoma Extramammary Paget's disease Vulvar intraepithelial neoplasia Bartholin gland carcinoma v t e Tumors of the male urogenital system Testicles Sex cord– gonadal stromal Sertoli–Leydig cell tumour Sertoli cell tumour Leydig cell tumour Germ cell G Seminoma Spermatocytic tumor Germ cell neoplasia in situ NG Embryonal carcinoma Endodermal sinus tumor Gonadoblastoma Teratoma Choriocarcinoma Embryoma Prostate Adenocarcinoma High-grade prostatic intraepithelial neoplasia HGPIN Small-cell carcinoma Transitional cell carcinoma Penis Carcinoma Extramammary Paget's disease Bowen's disease Bowenoid papulosis Erythroplasia of Queyrat Hirsuties coronae glandis
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Diastasis Symphysis Pubis
Wikipedia
Liesbeth Heuft-Dorenbosch1, René Weijers, Robert Landewé1, Sjef van der Linden1, Désirée van der Heijde1 External links [ edit ] Classification D MeSH : D046548 v t e Pathology of pregnancy , childbirth and the puerperium Pregnancy Pregnancy with abortive outcome Abortion Ectopic pregnancy Abdominal Cervical Interstitial Ovarian Heterotopic Embryo loss Fetal resorption Molar pregnancy Miscarriage Stillbirth Oedema , proteinuria and hypertensive disorders Gestational hypertension Pre-eclampsia HELLP syndrome Eclampsia Other, predominantly related to pregnancy Digestive system Acute fatty liver of pregnancy Gestational diabetes Hepatitis E Hyperemesis gravidarum Intrahepatic cholestasis of pregnancy Integumentary system / dermatoses of pregnancy Gestational pemphigoid Impetigo herpetiformis Intrahepatic cholestasis of pregnancy Linea nigra Prurigo gestationis Pruritic folliculitis of pregnancy Pruritic urticarial papules and plaques of pregnancy (PUPPP) Striae gravidarum Nervous system Chorea gravidarum Blood Gestational thrombocytopenia Pregnancy-induced hypercoagulability Maternal care related to the fetus and amniotic cavity amniotic fluid Oligohydramnios Polyhydramnios Braxton Hicks contractions chorion / amnion Amniotic band syndrome Chorioamnionitis Chorionic hematoma Monoamniotic twins Premature rupture of membranes Obstetrical bleeding Antepartum placenta Circumvallate placenta Monochorionic twins Placenta accreta Placenta praevia Placental abruption Twin-to-twin transfusion syndrome Labor Amniotic fluid embolism Cephalopelvic disproportion Dystocia Shoulder dystocia Fetal distress Locked twins Nuchal cord Obstetrical bleeding Postpartum Pain management during childbirth placenta Placenta accreta Preterm birth Postmature birth Umbilical cord prolapse Uterine inversion Uterine rupture Vasa praevia Puerperal Breastfeeding difficulties Low milk supply Cracked nipples Breast engorgement Childbirth-related posttraumatic stress disorder Diastasis symphysis pubis Postpartum bleeding Peripartum cardiomyopathy Postpartum depression Postpartum psychosis Postpartum thyroiditis Puerperal fever Puerperal mastitis Other Concomitant conditions Diabetes mellitus Systemic lupus erythematosus Thyroid disorders Maternal death Sexual activity during pregnancy Category v t e Dislocations / subluxations , sprains and strains Joints and ligaments Head and neck Dislocation of jaw Whiplash Shoulder and upper arm GH ( Dislocated shoulder ) AC ( Separated shoulder ) ALPSA lesion SLAP tear Bankart lesion Elbow and forearm Pulled elbow Gamekeeper's thumb Hip and thigh Hip dislocation Knee and leg Tear of meniscus Anterior cruciate ligament injury Unhappy triad Patellar dislocation Knee dislocation Ankle and foot Sprained ankle ( High ankle sprain ) Turf toe Muscles and tendons Shoulder and upper arm Rotator cuff tear Hip and thigh Pulled hamstring Knee and leg Patellar tendon rupture Achilles tendon rupture Shin splints
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Right-Sided Aortic Arch
Wikipedia
However when it is accompanied by other vascular abnormalities, it may form a vascular ring , causing symptoms due to compression of the trachea and/or esophagus . [1] Pathophysiology [ edit ] The causes of right-sided aortic arch are still unknown, 22q11 deletions have been found in some people with this condition. [2] It has also been found in association with other genetic syndromes such as Trisomy 21 (Down syndrome). ... External links [ edit ] Radiopaedia: Aortic arch variants eMedicine: Right Aortic Arch in Vascular Ring Defects v t e Congenital vascular defects / Vascular malformation Great arteries / other arteries Aorta Patent ductus arteriosus Coarctation of the aorta Interrupted aortic arch Double aortic arch Right-sided aortic arch Overriding aorta Aneurysm of sinus of Valsalva Vascular ring Pulmonary artery Pulmonary atresia Stenosis of pulmonary artery Subclavian artery Aberrant subclavian artery Umbilical artery Single umbilical artery Great veins Superior / inferior vena cava Congenital stenosis of vena cava Persistent left superior vena cava Pulmonary vein Anomalous pulmonary venous connection ( Total , Partial ) Scimitar syndrome Arteriovenous malformation Cerebral arteriovenous malformation
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Albuminuria
Wikipedia
Swelling of the ankles, hands, belly or face may occur if losses of albumin are significant and produce low serum protein levels ( nephrotic syndrome ). Causes [ edit ] The kidneys normally do not filter large molecules into the urine, so albuminuria can be an indicator of damage to the kidneys or excessive salt intake. ... Recent international guidelines ( KDIGO 2012 ) reclassified chronic kidney disease (CKD) based on cause, glomerular filtration rate category, and albuminuria category (A1, A2, A3). [1] Causes of albuminuria can be discriminated between by the amount of protein excreted. The nephrotic syndrome usually results in the excretion of about 3.0 to 3.5 grams per 24 hours. [ medical citation needed ] Nephritic syndrome results in far less albuminuria. [ medical citation needed ] Microalbuminuria (between 30 and 300 mg/24h, [2] mg/l of urine [3] or μg/mg of creatinine [4] ) can be a forerunner of diabetic nephropathy .ACE, INS, TNF, PTGS2, NCK1, TSLP, REN, LEPR, IL6, GNAQ, SOD2, MIR130A, GPC5, MIR145, NPHS1, NPHS2, MIR155, CP, MIR424, CD38, NCK2, CASP1, PYCARD, AGT, TRPC3, TRPC6, SPP1, SH2B3, PDPN, AGER, LRP2, CSF1, ALB, EDN1, CYP11B1, CTSL, CTSB, RAB38, CASR, BAHCC1, HOTTIP, ARL15, LINC00862, CHD7, C2orf83, FBXL20, SHROOM3, SPATA5L1, ICA1L, SBF2, LRMDA, ADO, AK5, LINC02752, MAPKBP1, CPS1, CCT2, CWC27, USP3, SNX17, NRXN1, CUBN, AHR, AQP7, COL4A4, NMU, PEX1, MYL3, GALT, FUT1, CCL2, DCN, CCL5, SELP, VEGFA, ADD1
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Retroverted Uterus
Wikipedia
Urologic Clinics of North America - Volume 34, Issue 1 (February 2007) ^ http://www.2womenshealth.com/23-Pelvic-Pain-and-Painful-Periods/23-28-Retroverted-Uterus.htm External links [ edit ] MedlinePlus Encyclopedia : 001506 Overview at mayoclinic.com Diagram at womens-health.co.uk Classification D ICD - 10 : N85.4 , O34.5 , O65.5 ICD - 9-CM : 621.6 MeSH : D019687 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
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Salpingitis
Wikipedia
External links [ edit ] Classification D ICD - 10 : N70 ICD - 9-CM : 614.2 MeSH : D012488 DiseasesDB : 9748 External resources eMedicine : med/2059 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
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Central Giant-Cell Granuloma
Wikipedia
Central giant-cell granulomas are more common in the anterior mandible , often crossing the midline and causing painless swellings. [1] Contents 1 Signs and symptoms 1.1 Noonan syndrome 2 Diagnosis 2.1 Histology 2.2 Differential diagnosis 3 Treatment 4 See also 5 References 6 External links Signs and symptoms [ edit ] CGCG is the most common giant cell lesion of the jaws. ... However, can be seen in a broad age range. [2] Noonan syndrome [ edit ] Multiple CGCGs can be found in individuals with Noonan syndrome .
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Urophagia
Wikipedia
Consumption of urine This article is part of a series on Alternative medicine General information Alternative medicine Alternative veterinary medicine Quackery (Health fraud) History of alternative medicine Rise of modern medicine Pseudoscience Antiscience Skepticism Skeptical movement National Center for Complementary and Integrative Health Terminology of alternative medicine Therapeutic nihilism Fringe medicine and science Acupressure Acupuncture Alkaline diet Anthroposophic medicine Apitherapy Applied kinesiology Aromatherapy Auriculotherapy Bates method Black salve Bodywork Bonesetter Bowen technique Breathwork Fake COVID-19 treatments Cancer treatments Charcoal cleanse Chiropractic Chiropractic treatment techniques Vertebral subluxation Christian Science Chromotherapy Colon cleansing Coffee enema Colorpuncture Colloidal silver Craniosacral therapy Crystal healing Cupping therapy Dental amalgam controversy Detoxification Foot detox Ear candling Energy medicine Esoteric energy Therapeutic touch Fabunan Antiviral Injection Facilitated communication Feldenkrais Method Functional medicine Hair analysis Herbal medicine Holistic dentistry Hologram bracelet Homeopathy Bach flower remedies Biological terrain assessment Hypnotherapy Iridology Ionized jewelry Jilly Juice Lightning Process Lymphotherapy Medical intuitive Mesmerism Magnet therapy Manual therapy Megavitamin therapy Mind–body interventions MMS Myofascial release NAET Naturopathy Oil pulling Orgone Orthomolecular medicine Orthopathy Osteomyology Osteopathy Ozone therapy Parapsychology Phrenology Psychic surgery Psychodermatology Radionics Rapid prompting method RBOP Reiki Reflexology Rolfing Scientific racism ThetaHealing Thought Field Therapy Urophagia Vaginal steaming Vision therapy Vitalism Young blood transfusion Zero balancing Conspiracy theories ( list ) Big Pharma conspiracy theory HIV/AIDS denialism OPV AIDS hypothesis Anti-vaccination Vaccines and autism MMR vaccine and autism Water fluoridation controversy GMO conspiracy theories Misinformation related to the COVID-19 pandemic Classifications Alternative medical systems Mind–body intervention Biologically-based therapy Manipulative methods Energy therapy Traditional medicine African Muti Southern Africa Ayurveda Ayurvedic acupressure Dosha Maharishi Vedic Approach to Health Balneotherapy Brazilian Bush medicine Cambodian Chinese Blood stasis Chinese herbology Dit Da Gua sha Gill plate trade Meridian Moxibustion Pressure point Qi San Jiao Tui na Zang-fu Chumash Curandero Faith healing Iranian Jamu Kambo Japanese Korean Mien Shiang Mongolian Prophetic medicine Shamanism Shiatsu Siddha Sri Lankan Thai massage Tibetan Unani Vietnamese Diagnoses Adrenal fatigue Aerotoxic syndrome Candida hypersensitivity Chronic Lyme disease Electromagnetic hypersensitivity Heavy legs Leaky gut syndrome Multiple chemical sensitivity Wilson's temperature syndrome v t e Urophagia is the consumption of urine .