Ectodermal dysplasia: Report of two cases in a family and literature review

Autor:	Vani Chappidi, Dheeraj Voulligonda, Bharadwaj Bhogavaram, P Krishnanjaneya Reddy
Jazyk:	angličtina
Rok vydání:	2019
Předmět:	Ectodermal dysplasia hypodontia hypohidrotic hypotrichosis Medicine
Zdroj:	Journal of Family Medicine and Primary Care, Vol 8, Iss 3, Pp 1263-1265 (2019)
Druh dokumentu:	article
ISSN:	2249-4863
DOI:	10.4103/jfmpc.jfmpc_48_19
Popis:	Ectodermal dysplasia (ED) is a inherited genetic disorder with manifestations of abnormalities in more than one ectodermal derivatives like skin, hair, nails, exocrine glands and teeth. There are more than 150 different variants of ED described in literature. The condition is thought to occur in approximately 1 in every 100,000 live births. It mainly manifests in two types i.e. Hypohidrotic (Anhidrotic) type and Hydrotic type depending on degree of sweat gland function. This report presents two cases within a family, a 4 year old boy and a 6 year old girl with typical features of Hypohidrotic Hereditary ED i.e, hypodontia, hypohidrosis and hypotrichosis.
Databáze:	Directory of Open Access Journals
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