A first case report of hypohidrotic ectodermal dysplasia from Oman

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Abstract

This is a first case report of a patient with hypohidrotic ectodermal dysplasia from Oman, who was found to carry a mutation in the EDAR gene after candidate gene selection based on regions of homozygosity in his genome.

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Al-Araimi, M., Hamza, N., Al Hosni, A., & Al Mazrooey, H. (2020). A first case report of hypohidrotic ectodermal dysplasia from Oman. Clinical Case Reports, 8(4), 716–718. https://doi.org/10.1002/ccr3.2723

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