Prader-Willi syndrome


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Related to Prader-Willi syndrome: Cushing's syndrome, phenylketonuria, Williams syndrome, Angelman syndrome, Rett syndrome, Turner syndrome

Pra·der-Wil·li syndrome

 (prä′dər-vĭl′ē)
n.
A genetic disorder characterized by short stature, intellectual disability, involuntary craving for food with subsequent obesity, behavior and learning problems, and incomplete sexual development.

[After Andrea Prader (1919-2001), Swiss pediatrician and endocrinologist, and Heinrich Willi (1900-1971), Swiss pediatrician.]

Prader-Willi syndrome

(ˌprɑːdəˈvɪlɪ)
n
(Medicine) a congenital condition characterized by obsessive eating, obesity, mental retardation, and small genitalia
[C20: after Andrea Prader (1919–2001) and Heinrich Willi (1900–71), Swiss paediatricians]
References in periodicals archive ?
A Phase 2 setmelanotide trial is ongoing for the treatment of Prader-Willi syndrome (PWS), a rare genetic disorder that causes life-threatening obesity.
Their condition could be due to endocrinal disease or Prader-Willi syndrome, but we can only ascertain the right treatment after a proper diagnosis at one of our top hospitals.
Prader-Willi syndrome is a condition that leads to poor muscle tone, motor skills, difficulties in learning, behavioural problems, short physique, decreased production of sex hormones, hunger, and obesity.
Now Isabella's parents Stuart and Helen Bailey, from Northumberland Park, North Tyneside, have completed a walk to raise money for the Prader-Willi Syndrome Association UK.
Activity there kicked on in most of the participants, except for those with Prader-Willi syndrome.
It is also administered to children who fail to grow because of chronic renal insufficiency or significant genetic abnormalities, including Turner syndrome, Noonan syndrome, and Prader-Willi syndrome.
Three-year-old Rhun Edwards, of Porthmadog, suffers from Prader-Willi Syndrome, which affects muscle growth, and leaves many sufferers confined to a wheelchair.
Prader-Willi syndrome (PWS) was chosen as a welldefined genetic model since it may help explain certain neurophysiological mechanisms that affect appetite and food addiction, which eventually lead to obesity, especially in children and young adults (von Deneen, Gold & Liu 2009).
Grace, of Lentons Lane, Holbrooks, Coventry was born with Prader-Willi syndrome, which affects muscle tone and increases appetite.
Dr Malcolm Donaldson, an endocrine pediatrician, runs a clinic at Yorkhill Hospital in Glasgow for the Prader-Willi Syndrome and the proceeds of the show will go to the Prader-Willi Syndrome Association UK.
The current accepted evidence-based indications for GH are GH deficiency, Turner syndrome, Prader-Willi syndrome, small-for-gestational-age children who fail to show catch-up growth, idiopathic short stature, and chronic renal failure.