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VOLUME 7 , ISSUE 1 ( January-April, 2019 ) > List of Articles

CASE REPORT

Ectodermal Dysplasia—A Case Report

Damanpreet Kaur, Ashima Behl, Parminder Pal Singh Isher, Dipti Bhatnagar

Keywords : ectodermal dysplasia, anodontia, hypohidrosis, hypotrichosis

Citation Information : Kaur D, Behl A, Isher PP, Bhatnagar D. Ectodermal Dysplasia—A Case Report. 2019; 7 (1):38-41.

DOI: 10.1055/s-0039-1684943

License: CC BY-NC-ND 4.0

Published Online: 04-04-2019

Copyright Statement:  © 2019 Bhojia Dental College and Hospital affiliated to Himachal Pradesh University


Abstract

Ectodermal dysplasias (EDs) include large group of syndromes that are clinically and genetically heterogeneous and are identified by anomalies in structures of ectodermal origin. Hereditary ectodermal dysplasia is a condition associated with defect of structures originating from ectoderm and is typically inherited as cross-linked recessive trait, more pronounced in males than in females. The frequency of different ectodermal dysplasias in a given population is highly variable. It is estimated to be 7 in 1,000 births. This case report is presented with an objective to show two patients, siblings, with ED. Both presented with classic symptoms of anodontia, hypohidrosis, and hypotrichosis.

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