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Sakati–Nyhan–Tisdale syndrome : ウィキペディア英語版 | Sakati–Nyhan–Tisdale syndrome
Sakati–Nyhan–Tisdale syndrome,〔(【引用サイトリンク】 publisher = Ole Daniel Enersen )〕 also called acrocephalopolysyndactyly type III, is a rare genetic disorder that has been associated with abnormalities in the bones of the legs, congenital heart defects and craniofacial defects. The syndrome belongs to a group of rare genetic disorders known as acrocephalopolysyndactyly or ACPS, for short.〔(【引用サイトリンク】 publisher = WebMD )〕 ==Eponym== The disease was named after a Syrian pediatrician named Nadia Awni Sakati〔(【引用サイトリンク】 author = Patrick Jucker-Kupper )〕 and her two American counterparts, William Leo Nyhan〔(【引用サイトリンク】 author = Günter Krämer )〕 and W.K. Tisdale,〔(【引用サイトリンク】 publisher = Ole Daniel Enersen )〕 who were working alongside her in the pediatrics department at University of California, San Diego. It was characterized in 1971.
抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)』 ■ウィキペディアで「Sakati–Nyhan–Tisdale syndrome」の詳細全文を読む
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