|
プラダーウィリ症候群
先天性遺伝子オレゴン
[慢性]
体重増加, 発達の遅れ, 肥満, 食欲旺盛
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. It was first described in 1956 by Andrea Prader, Heinrich Willi, Alexis Labhart, Andrew Ziegler, and Guido Fanconi of Switzerland.
|
|
検索編集
新しい検索