Presentation of hypohidrotic ectodermal dysplasia in two siblings | Zendy

Uday Ginjupally | Zendy; BalajiBabu Bangi | Zendy; Lavanya Gadapa | Zendy; Pooja Madki | Zendy

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Presentation of hypohidrotic ectodermal dysplasia in two siblings

Author(s) -

Uday Ginjupally,

BalajiBabu Bangi,

Lavanya Gadapa,

Pooja Madki

Publication year - 2015

Publication title -

journal of indian academy of oral medicine and radiology

Language(s) - English

Resource type - Journals

eISSN - 0975-1572

pISSN - 0972-1363

DOI - 10.4103/0972-1363.170465

Subject(s) - hypohidrotic ectodermal dysplasia , hypodontia , ectodermal dysplasia , hypotrichosis , medicine , dermatology , dentistry , genetics , biology , gene

Ectodermal dysplasias are a large hereditary group of disorders which are usually manifested as X-linked recessive disorders and have a full expression in males, whereas females show little to no signs of the disorder. The two most common types of ectodermal dysplasias are hypohidrotic ectodermal dysplasia (Christ-Siemens-Touraine syndrome) and hidrotic ectodermal dysplasia (Clouston syndrome). Hypohidrotic ectodermal dysplasia is characterized by hypodontia, hypotrichosis, and hypohidrosis. Here, we present two female sibling cases of hypohidrotic ectodermal dysplasia

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