Definición de Prader–Willi syndrome en inglés:

Prader–Willi syndrome

Saltos de línea: Prader–Willi syn|drome
Pronunciación: /ˌprɑːdəˈvɪli
 
/

sustantivo

[mass noun]
A rare congenital disorder characterized by learning difficulties, growth abnormalities, and obsessive eating, caused especially by the absence of certain genes normally present on the copy of chromosome 15 inherited from the father.

Origen

1960s: named after Andrea Prader (born 1919) and Heinrich Willi (1900–71), Swiss paediatricians.

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