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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 Naegeli–Franceschetti–Jadassohn syndrome ： ウィキペディア英語版 Naegeli–Franceschetti–Jadassohn syndrome Naegeli–Franceschetti–Jadassohn syndrome (NFJS), also known as chromatophore nevus of Naegeli and Naegeli syndrome, is a rare autosomal dominant form of ectodermal dysplasia, characterized by reticular skin pigmentation, diminished function of the sweat glands, the absence of teeth and hyperkeratosis of the palms and soles. One of the most striking features is the absence of fingerprint lines on the fingers. Naegeli syndrome is similar to Dermatopathia pigmentosa reticularis, both of which are caused by a specific defect in the keratin 14 protein. ==Cause and Genetics== NFJS is caused by mutations in the keratin 14 (KRT14) gene, located on chromosome 17q12-21.〔 The disorder is inherited in an autosomal dominant manner, which means that the defective gene responsible for a disorder is located on an autosome (chromosome 17 is an autosome), and only one copy of the defective gene is sufficient to cause the disorder, when inherited from a parent who has the disorder. 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「Naegeli–Franceschetti–Jadassohn 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.