X-linked Hypohidrotic Ectodermal Dysplasia
What's New
Last Posted: Mar 05, 2023
- EDA, EDAR, EDARADD and WNT10A allelic variants in patients with ectodermal derivative impairment in the Spanish population.
Martínez-Romero María Carmen, et al. Orphanet journal of rare diseases 2019 0 (1) 281 - [Prenatal diagnosis of a fetus with X-linked hypohidrotic ectodermal dysplasia].
Duan Fuhua, et al. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2020 0 (11) 1269-1271 - No evidence for preferential X-chromosome inactivation as the main cause of divergent phenotypes in sisters with X-linked hypohidrotic ectodermal dysplasia.
Körber Laura, et al. Orphanet journal of rare diseases 2021 0 (1) 98 - Prenatal Correction of X-Linked Hypohidrotic Ectodermal Dysplasia.
Schneider Holm et al. The New England journal of medicine 2018 Apr (17) 1604-1610 - Protein therapy in the womb overrides genetic glitch hampering teeth development, ability to sweat
R Lewis, Genetic Literacy Project, Apr 25, 2018 - Sweating ability and genotype in individuals with X-linked hypohidrotic ectodermal dysplasia.
Schneider Holm, et al. Journal of medical genetics 2011 6 (6) 426-32 - X-linked hypohidrotic ectodermal dysplasia
From NCATS Genetic and Rare Diseases Information Center
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