Hypohidrotic ectodermal dysplasia: A case report

被引：0
|
作者：
Kumar, Vagish L. S. [1 ]
机构：
[1] Yenepoya Univ, Yenepoya Res Ctr, Dept Oral Med & Radiol, Yenepoya Dent Coll & Hosp, Mangalore 575018, Karnataka, India
来源：
EUROPEAN JOURNAL OF THERAPEUTICS | 2015年 / 21卷 / 02期
关键词：
Christ-Siemens Touraine syndrome; ectodermal dysplasia; hypohidrosis; missing teeth;
D O I：
10.5455/GMJ-30-172543
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
Ectodermal dysplasia is a hereditary disorder exhibiting developmental abnormalities of ectodermal structures. Patients with these disorders usually exhibit multiple missing teeth, sparse hair and inability to sweat with other manifestations. Early recognition and treatment by clinicians will prevent development of psychological trauma in patient and gives confidence to the patient. The current article presents a case of a 28 year old male with hypohidrotic ectodermal dysplasia who presented with rare unusual hyperpigmentations.
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收藏
页码：154 / 157
页数：4
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