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1,879 Possible Causes for Prader-Willi Syndrome

  • Hypogonadism

    ., Klinefelter syndrome, hemochromatosis, Kallmann syndrome, Prader-Willi syndrome, and mytonic dystrophy) can also cause low testosterone.[] Laurence-Moon syndrome, isolated luteinizing hormone deficiency, Prader-Willi syndrome, and functional and acquired disorders of the CNS (eg, trauma, infection).[] Patients with Prader-Willi syndrome may be treated with human growth hormone. Several studies have shown this treatment is beneficial.[]

  • Morbid Obesity

    The findings of morbid obesity, anasarca, self-injury, hyperuricemia and hypoxemia in Prader-Willi syndrome are emphasized.[] Prader-Willi syndrome (PWS) is a rare genetic disorder that affects about 1 in 14,000 people in the United States.[] […] childbirth and the puerperium, if applicable ( O99.21- ) Type 1 Excludes adiposogenital dystrophy ( E23.6 ) lipomatosis NOS ( E88.2 ) lipomatosis dolorosa [Dercum] ( E88.2 ) Prader-Willi[]

  • Laurence Moon Syndrome

    】 多腺性自己免疫症候群 【 polyuria 】 多尿 【 Prader-Willi syndrome 】 プラダー・ウィリー症候群 【 primary aldosteronism 】 原発性アルドステロン症 【 progesterone 】 プロゲステロン 【 prolactin (PRL) 】 プロラクチン 【 prolactinoma[] プラダー・ウィリ Prader-Willi syndrome プラダー・ウィリ症候群 AndreaPrader (1919-2001) Swiss pediatrician and endocrinologist and Heinrich Willi(1900-1971) Swiss pediatrician Prausnitz-Kustner[] 副甲状腺ホルモン関連ペプチド 【 periodic paralysis 】 周期性四肢麻痺 【 pheochromocytoma 】 褐色細胞腫 【 pituitary adenoma 】 下垂体腺腫 【 Plummer disease 】 プラマー病 【 polydipsia 】 多飲 【 polyglandular autoimmune syndrome[]

  • 17q11 Microdeletion Syndrome

    Partial acquired lipodystrophy Partial androgen insensitivity syndrome Partial atrioventricular canal Prader-Willi syndrome due to imprinting mutation Prader-Willi syndrome[] 22q13.3, SHANK3, ACR, RABL2B P188 Prader Willi syndrome (PWS), Angelman syndrome (AS) PWS/AS region (15q11-13), MKRN3, MAGEL2, NDN, SNRPN, UBE3A, ATP10A, GABRB3, OCA2 ME028[] ; Ptls 610883 RAI1, MFAP4, FLII 17p11.2 Potocki-Shaffer Syndrome 601224 ALX4, EXT2 11p11.2 Prader-Willi Syndrome; Pws 176270 SIM1 6q16.3 Prader-Willi Syndrome; Pws 176270[]

  • Familial Short Stature

    GENETIC SYNDROME : Turner syndrome, Noonan syndrome, Silver-Russel syndrome, DiGeorge syndrome, Prader Willi Syndrome, Down syndrome, Shwachman-Diamond Syndrome Short stature[] “Endocrine and metabolic aspects of Prader-Willi syndrome”. Management of Prader-Willi Syndrome. 1995. pp. 32-57. (Review of PWS.)[] Prader-Willi syndrome (PWS) What you should be alert for in the history Prader-Willi syndrome (PWS) is a rare genetic disorder occurring in 1:10,000 to 1:25,000 individuals[]

  • Angelman Syndrome

    We report on a 32-y-old woman with Prader-Willi syndrome (PWS) and her daughter with Angelman syndrome (AS).[] As she grew older, indications of phenotypical traits similar to Prader-Willi syndrome (PWS) appeared, in particular hyperphagic behavior and a body fat distribution similar[] Angelman syndrome (AS) and Prader-Willi syndrome (PWS) are distinct human neurogenetic disorders; however, a clinical overlap between AS and PWS has been identified.[]

  • Obesity Hypoventilation Syndrome

    Fourteen children with the Prader-Willi syndrome have been managed at the Royal Alexandra Hospital for Children between the years 1964-1980--twelve male, two female.[] We studied ventilatory response to hypercapnia in the families of 2 obese 13-year-old girls with the Prader-Willi Syndrome, one of whom had recovered from the obesity hypoventilation[] Respirology. 2012; 17(5): 759-771 5 Genetic diseases: Congenital central hypoventilation, rett, and prader-willi syndromes Gallego, J.[]

  • Overeating

    In fact, your brain will start sending you signals to tell you you're full (unless you have Prader-Willi syndrome , a disorder that causes feelings of constant, ravenous hunger[]

  • Strabismus

    […] trisomy 18, cerebral palsy and Prader-Willi syndrome can also predispose children and adults to develop such a condition.[] syndrome Noonan syndrome Prader-Willi syndrome Retinopathy of prematurity Retinoblastoma Traumatic brain injury Trisomy 18 Strabismus that develops in adults can be caused[] , Prader-Willi syndrome, traumatic brain injury, incontinentia iigmenti syndrome, trisomy 18 and development of hemangioma near the eye during infancy.[]

  • Prader-Willi Syndrome

    Prader-Labhart-Willi syndrome PWS Willi-Prader syndrome Bittel DC, Butler MG. Prader-Willi syndrome: clinical genetics, cytogenetics and molecular biology.[] Prader-Willi Syndrome. 1998 Oct 6 [updated 2016 Feb 4].[] Prader-Willi syndrome (PWS), also known as Prader-Labhart-Willi syndrome, is a rare genetic disorder that arises due to genetic abnormalities.[]

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