A case of anodontia with ectodermal dysplasia on the siblings

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منابع مشابه

Hypohidrotic Ectodermal Dysplasia with Total Anodontia: A Case Report

Ectodermal dysplasia is a hereditary disorder that occurs as a consequence of disturbances in the ectoderm of the developing embryo. The triad of nail dystrophy, alopecia or hypotrichosis and palmoplantar hyperkeratosis is usually accompanied by a lack of sweat glands and a partial or complete absence of primary and/ or permanent dentition. A case report illustrating the prosthetic rehabilitati...

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Ectodermal Dysplasia with Anodontia: A Report of Two Cases

Ectodermal dysplasia is a hereditary disorder that occurs as a consequence of disturbances in the ectoderm of the developing embryo. The triad of nail dystrophy, alopecia or hypotrichosis and palmoplantar hyperkeratosis is usually accompanied by a lack of sweat glands and a partial or complete absence of primary and/or permanent dentition. Two case reports illustrating the prosthetic rehabilita...

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[Oligodontia in 2 siblings with ectodermal dysplasia].

Oligodontia, a form of hypodontia, is commonly seen in permanent than in deciduous dentition. It is defined as the congenital absence of six or more teeth, excluding third molars. It is relatively a rare condition which occurs as an isolated finding or as part of a syndrome. The present paper shows a rare case of oligodontia with ectodermal dysplasia in 2 siblings (boys). Both the cases were as...

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Anodontia with hypohidrotic ectodermal dysplasia in a young female: a case report.

A five-year-old Japanese girl was referred to our clinic for non-eruption of the teeth. Panoramic radiographs revealed absence of all teeth of both primary and permanent dentitions. She showed hypotricosis, hypohidrosis, and anodontia. In this article, the reported cases of anodontia were reviewed and the fabricating procedure of full dentures for a young child was described.

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ژورنال

عنوان ژورنال: Japanese Journal of Oral & Maxillofacial Surgery

سال: 1980

ISSN: 2186-1579,0021-5163

DOI: 10.5794/jjoms.26.1030