Hypohydrotic ectodermal dysplasia -a case report.

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dc.contributor.authorRao, V Arun Prasad
dc.contributor.authorReddy, N Venugopal
dc.contributor.authorKrishana, R
dc.contributor.authorSugumaran, D K
dc.contributor.authorPallavi, Pandey
dc.contributor.authorPari, Arul
dc.date.accessioned2016-02-22T08:55:04Z
dc.date.available2016-02-22T08:55:04Z
dc.date.issued2010-04
dc.description.abstractEctodermal dysplasia is a rare hereditary disorder. Its Hypohidrotic (HED) variant is also known as Chirst- Siemens-Touraine syndrome. It is inherited as an X- linked trait. Such Patients are characterized by the clinical manifestations of Hypodontia, Hypotrichosis, Hypohidrosis and a highly characteristic facial physiognomy. This article, reports a typical case of Hypohidrotic Ectodermal Dysplasia (HED) and management.en_US
dc.identifier.citationRao V Arun Prasad. Reddy N Venugopal, Krishana R, D K Sugumaran, Pallavi Pandey, Pari Arul. Hypohydrotic ectodermal dysplasia -a case report .Annals and Essences of Dentistry. 2010 Apr-June; 2(2): 31-35.en_US
dc.identifier.issn0975-8798
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/173795
dc.language.isoenen_US
dc.source.urihttps://www.aedj.in/index.php?title=2.2.31-35&action=edit&redlink=1en_US
dc.subjectEctodermal dysplasiaen_US
dc.subjectHypohidrotic ectodermal dysplasiaen_US
dc.subjectHypodontiaen_US
dc.subjectHypotrichosien_US
dc.titleHypohydrotic ectodermal dysplasia -a case report.en_US
dc.typeArticleen_US
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