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Illness finder is a diagnostic medicine tool for educational purpose that looks up your patients' health conditions or symptoms and diagnosis and find diseases or illnesses based on chosen gender, age, risk factors, illness, signs, symptoms and prevalence. Illnessfinder is inspired by Evidence based medicine (EMB) and healthcare that aims to apply the best (most reliable) knowledge that is available at decision time. Illnessfinder aims to free up time for the therapeutic dialogue and ensure quality at the evidence based practice, uniting proven medical findings and clinical evidence with systematised data technology.
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| Prader-Willi Syndrome | Legal notice |
Other terms
Prader Willi Syndrome,Syndrome, Prader-Willi,Labhart-Willi-Prader-Fanconi Syndrome,Labhart Willi Prader Fanconi Syndrome,Syndrome, Labhart-Willi-Prader-Fanconi,Willi-Prader Syndrome,Syndrome, Willi-Prader,Willi Prader Syndrome,Labhart-Willi Syndrome,Labhart Willi Syndrome,Syndrome, Labhart-Willi,Prader Labhart Willi Syndrome,Royer Syndrome,Syndrome, Royer,Royer's Syndrome,Royers Syndrome,Syndrome, Royer's
Description
Prader-Willi Syndrome: An autosomal dominant disorder caused by deletion of the proximal long arm of the paternal chromosome 15 (15q11-q13) or by inheritance of both of the pair of chromosomes 15 from the mother (UNIPARENTAL DISOMY) which are imprinted (GENETIC IMPRINTING) and hence silenced. Clinical manifestations include MENTAL RETARDATION; MUSCULAR HYPOTONIA; HYPERPHAGIA; OBESITY; short stature; HYPOGONADISM; STRABISMUS; and HYPERSOMNOLENCE. (Menkes, Textbook of Child Neurology, 5th ed, p229)
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Legal notice
The U.S. National Library of Medicine is the creator, maintainer, and provider of the data above.
The version of the data is 2010 MeSH. Last reviewed April 26, 2010. No modification has been made in the content of the file.
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