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Urban–Rogers–Meyer syndrome : ウィキペディア英語版 | Urban–Rogers–Meyer syndrome
Urban–Rogers–Meyer syndrome, also known as Prader–Willi habitus, osteopenia, and camptodactyly or Urban syndrome, is an extremely rare inherited congenital disorder first described by Urban et al. (1979). It is characterized by genital anomalies, mental retardation, obesity, contractures of fingers, and osteoporosis,〔 though further complications are known.〔(【引用サイトリンク】title=Urban Rogers Meyer syndrome )〕 ==References==
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「Urban–Rogers–Meyer syndrome」の詳細全文を読む
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