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Hypohidrotic Ectodermal Dysplasia with total anodontia: a case report
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- Journal of Clinical and Experimental Dentistry
- Journal of Clinical and Experimental Dentistry. 2011. Vol. 3, no. 4-1
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Hypohidrotic Ectodermal Dysplasia with total anodontia: a case report
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| Shashibhushan, K.K.; Viswanathan, Revathy; Sathyajith Naik, N.; Subba Reddy, V.V. | |||
| Aquest document és un/a article, creat/da en: 2011 | |||
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| 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 rehabilitation of a seven year old boy with hypohidrotic ectodermal dysplasia associated with total anodontia is presented. | |||
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