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Hypohidrotic Ectodermal Dysplasia - Genetics Home Reference Hypohidrotic ectodermal dysplasia is one of about 150 types of ectodermal dysplasia in humans. Before birth, these disorders result in the abnormal development of structures http://ghr.nlm.nih.gov/condition=hypohidroticectodermaldysplasia
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Ectodermal Dysplasia Ectodermal dysplasia is a hereditary condition characterized by abnormal development of the skin and associated structures (hair, nails and teeth, and sweat glands). http://www.phoebeputney.com/information/healthlibrary/hie/001469.asp
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Ectodermal Dysplasia. Department of Oral Medicine, Laval University, SteFoy, Province of Quebec, Canada. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1029900/
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Hypohidrotic Ectodermal Dysplasia GeneReviews NCBI Bookshelf GeneReviews designates a molecular genetic test as clinically available only if the test is listed in the GeneTests Laboratory Directory by either a US CLIAlicensed laboratory http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=x-hed