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Autosomal hypohidrotic ectodermal dysplasia
- ... WNT10A gene can cause either autosomal dominant or autosomal recessive hypohidrotic ectodermal dysplasia.Autosomal dominant inheritance means one copy of the ...
- ... EDAR genes underlie X-linked isolated hypodontia and autosomal recessive hypohidrotic ectodermal dysplasia. Arch Dermatol Res. 2009 Sep;301(8):625- ... EDAR gene in two Pakistani consanguineous families with autosomal recessive hypohidrotic ectodermal dysplasia. Br J Dermatol. 2005 Jul;153(1):46- ...
- ... of two alternate cryptic 5'-splice sites causes autosomal recessive Hypohidrotic Ectodermal Dysplasia. Am J Med Genet A. 2016 Jun;170( ...
- ... NFKBIA gene, the condition is inherited in an autosomal dominant pattern, which means one ... Ectodermal dysplasia, hypohidrotic, with immune deficiency EDA-ID HED-ID Hyper- ...
- ... the WNT10A gene have been found to cause hypohidrotic ectodermal dysplasia, the most common form of ectodermal dysplasia. Starting ... the skin, hair, nails, teeth, and sweat glands. Hypohidrotic ectodermal dysplasia is characterized by a reduced ability to sweat ( ...