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frequency
uncommon (U.S.)
likelihood by age
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Definition for Prader-Willi Syndrome

Prader-Willi Syndrome is a genetic disorder in which seven genes (or some subset thereof) on chromosome 15 are missing or unexpressed (chromosome 15q partial deletion) on the paternal chromosome. more


some common symptoms
delayed development
increased appetite
obese
weight gain


some related diagnoses
1 - 7 of 14 diagnoses
Pickwickian Syndrome
Hyperlipoproteinemia Type III
obstructive sleep apnea
diabetes mellitus type 2
asthma
hypertensive heart disease
hypertension
  more

do i have 'Prader-Willi Syndrome'?
In addition the following diagnostic tests might be need to help verify the diagnosis:
diagnostic test search results for 'prader-willi syndrome'
1 - 5 of 28 diagnostic tests
Molecular Genetic Studies
Arterial Blood Gas
Chest X-ray
Radiological technique to image the chest
Complete metabolic panel
Polysomnogram
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therapeutic procedures for 'Prader-Willi Syndrome'?
Managing or treating a diseases should always be determined by a patients health care provider. Below is a list of associated therapeutic procedures or medications for Prader-Willi Syndrome:
therapeutic procedure search results for 'prader-willi syndrome'
1 - 2 of 2 therapeutic procedures
rankings are computer generated. please consult your health care provider.
Maintain Healthy Weight
Oxygen


medications search results for 'prader-willi syndrome'
1 - 1 of 1 medications
rankings are computer generated. please consult your health care provider.
  Human growth hormone



web search results for prader-willi syndrome
Results 1 - 50 - Prader-Willi Syndrome
en.wikipedia.org - summary
ghr.nlm.nih.gov - summary
www.nlm.nih.gov - summary
www.ncbi.nlm.nih.gov - summary
www.medicinenet.com - summary
www.ncbi.nlm.nih.gov - summary







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