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  1. Prader–Willi syndrome

    • IPA[ˌprɑːdəˈvɪlɪ ˌsɪndrəʊm]

    英式

    • n.
      a rare congenital condition characterized by excessive appetite, often leading to morbid obesity, and a variety of other signs including intellectual disability, short stature, and underdevelopment of the sexual organs, caused especially by the absence of certain genes normally present on the copy of chromosome 15 inherited from the father.
    • noun: Prader–Willi syndrome

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