关键词: Ectodermal dysplasia embryonic life genetic disorder hypohidrotic

来  源:   DOI:10.4103/jomfp.jomfp_287_21   PDF(Pubmed)

Abstract:
Ectodermal dysplasia represents a group of inherited conditions in which two or more ectodermally derived anatomical structures fail to develop resulting in most notably anhidrosis/hypohidrosis, hypotrichosis and hypodontia. It is a xlinked recessive disorder with male predominance. We report a classical case in a 17-year-old male with emphasis on review of literature and latest updates.
摘要:
外胚层发育不良代表一组遗传性疾病,其中两个或多个外胚层来源的解剖结构无法发育,导致最明显的无汗症/无汗症。少突症和少突症。这是一种以男性为主的连锁隐性疾病。我们报告了一个17岁男性的经典病例,重点是文献回顾和最新更新。
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