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Prader-Willi syndrome

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Prader-Willi syndrome [¦präd·ər ¦wil·ē ′sin‚drōm]
(medicine)
A genetic disorder that is caused by defects on the paternally derived chromosome 15, causing mild mental retardation, neonatal hypotonia, hypogonadism, compulsive overeating, childhood onset obesity, and mild facial dysmorphism.


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Megan Rose Lindon, who suffers from Prader-Willi Syndrome and uses a wheelchair, was visiting the store with her grandmother, Dorothy Taylor, to buy a uniform for the start of the new term in September.
After six weeks in special care, Dr James broke the news that Callum had Prader-Willi Syndrome (PWS), a condition that is often marked by learning difficulties, behavioural prob-lemand obesity.
CONTEXT: GH replacement in Prader-Willi syndrome (PWS) children has well-defined benefits and risks and is used extensively worldwide.
 
 
 
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