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遗传性少汗型外胚层发育不良:1例罕见病例报告。

Hereditary hypohidrotic ectodermal dysplasia: report of a rare case.

作者信息

Paramkusam Geetha, Meduri Venkateswarlu, Nadendla Lakshmi Kavitha, Shetty Namratha

机构信息

Professor & HOD, Department of Oral Medicine and Radiology, Kamineni Institute of Dental Sciences , Sreepuram, Narketpally, Nalgonda District, Andhra Pradesh - 508254, India .

出版信息

J Clin Diagn Res. 2013 Sep;7(9):2074-5. doi: 10.7860/JCDR/2013/5757.3409. Epub 2013 Sep 10.

Abstract

Hereditary Hypohidrotic Ectodermal Dysplasia (HHED), an X-linked, recessive, Mendelian character, is seen usually in males and it is inherited through female carriers. It is characterised by congenital dysplasia of one or more ectodermal structures and it is manifested by hypohidrosis, hypotrichosis and hypodontia. It results from abnormal morphogenesis of cutaneous and oral embryonic ectoderm. Here, we are presenting a rare case of HHED in a 19 year female with classic features of this condition.

摘要

遗传性少汗性外胚层发育不良(HHED)是一种X连锁隐性孟德尔性状,通常见于男性,通过女性携带者遗传。其特征为一个或多个外胚层结构的先天性发育异常,表现为少汗、毛发稀少和牙齿发育不全。它是由皮肤和口腔胚胎外胚层的形态发生异常引起的。在此,我们报告一例19岁女性的罕见HHED病例,该患者具有该病的典型特征。

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