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Hypohidrotic Ectodermal Dysplasia (ED): A Case Series

Identifieur interne : 000728 ( Main/Exploration ); précédent : 000727; suivant : 000729

Hypohidrotic Ectodermal Dysplasia (ED): A Case Series

Auteurs : Mallika Kishore ; Sunil R. Panat ; Ashish Aggarwal ; Nupur Agarwal ; Nitin Upadhyay ; Kratika Ajai ; Abhijeet Alok

Source :

RBID : PMC:3939504

Abstract

Ectodermal Dysplasia (ED) is a rare disorder with defects in two or more of the following structures: the teeth and the skin and its appendages including hair, nails, eccrine, and sebaceous glands. Dental manifestations include hypodontia, complete anodontia or malformed teeth. The most common form of the ED syndrome is hypohidrotic ED and is usually inherited as an X-linked recessive trait. Female carriers may have a variable degree of clinical manifestations. The condition is thought to occur in approximately 1 in every 100,000 live births. Dental treatment for these patients varies on an individual basis. Children with ED are often treated dentally with conventional adult appearing prosthesis which are focused only on the oral manifestations of the syndrome. We are here reporting two classical cases of hypohidrotic ED with a review of the literature.


Url:
DOI: 10.7860/JCDR/2014/6597.3951
PubMed: 24596794
PubMed Central: 3939504


Affiliations:


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