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Pediatr Dermatol ; 34(2): 172-175, 2017 Mar.
Article in English | MEDLINE | ID: mdl-28297138

ABSTRACT

Pure hair and nail ectodermal dysplasia (PHNED) is a rare disorder that presents with hypotrichosis and nail dystrophy while sparing other ectodermal structures such as teeth and sweat glands. We describe a homozygous novel missense mutation in the HOXC13 gene that resulted in autosomal recessive PHNED in a Hispanic child. The mutation c.812A>G (p.Gln271Arg) is located within the DNA-binding domain of the HOXC13 gene, cosegregates within the family, and is predicted to be maximally damaging. This is the first reported case of a missense HOXC13 mutation resulting in PHNED and the first reported case of PHNED identified in a North American family. Our findings illustrate the critical role of HOXC13 in human hair and nail development.


Subject(s)
Ectodermal Dysplasia/genetics , Homeodomain Proteins/genetics , Mutation, Missense/genetics , Ectodermal Dysplasia/pathology , Humans , Infant , Male , Pedigree
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