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翻訳と辞書　辞書検索 [ 開発暫定版 ] スポンサード リンク Ho–Kaufman–Mcalister syndrome ： ウィキペディア英語版 Ho–Kaufman–Mcalister syndrome Ho–Kaufman–Mcalister syndrome, also known as the Chen-Kung Ho–Kaufman–Mcalister syndrome, is a rare congenital malformation syndrome where infants are born with a cleft palate, micrognathia, Wormian bones, congenital heart disease, dislocated hips, bowed fibulae, preaxial polydactyly of the feet, abnormal skin patterns, and most prominently, missing tibia. The etiology is unknown. Ho–Kaufman–Mcalister syndrome is named after Chen-Kung Ho, R.L. Kaufman, and W.H. Mcalister who first described the syndrome in 1975 at Washington University in St. Louis. It is considered a rare disease by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). ==References== (Ho–Kaufman–Mcalister Syndrome Summary at PubMed ) Ho CK, Kaufman RL, Mcalister WH (1975). "Congenital Malformations: Cleft Palate, Congenital Heart Disease, Absent Tibiae, and Polydactyly." ''American Journal of Diseases of Children'' 1975 Jun. 129(6):714–6. 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「Ho–Kaufman–Mcalister syndrome」の詳細全文を読む スポンサード リンク 翻訳と辞書 : 翻訳のためのインターネットリソース Copyright(C) kotoba.ne.jp 1997-2016. All Rights Reserved.