Hypohidrotic ectodermal dysplasias

EDA mutation as a cause of hypohidrotic ectodermal dysplasia: a case report and review of the literature

S. X. Huang, Liang, J. L., Sui, W. G., Lin, H., Xue, W., Chen, J. J., Zhang, Y., Gong, W. W., Dai, Y., and Ou, M. L., EDA mutation as a cause of hypohidrotic ectodermal dysplasia: a case report and review of the literature, vol. 14, pp. 10344-10351, 2015.

Ectodermal dysplasia (ED) represents a collection of rare disorders that result from a failure of development of the tissues derived from the embryonic ectoderm. ED is often associated with hair, teeth, and skin abnormalities, which are serious conditions affecting the quality of life of the patient. To date, a large number of genes have been found to be associated with this syndrome. Here, we report a patient with hypohidrotic ED (HED) without family history.

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