Abstract:
Pure hair and nail ectodermal dysplasia (PHNED) is a rare genetic disorder characterized by hypotrichosis or complete alopecia, as well as nail dystrophy. Mutations in the type II hair keratin gene KRT85 and the HOXC13 gene on chromosome 12q have recently been identified in families with autosomal-recessive PHNED. In the present study, we have analyzed a consanguineous Syrian family with an affected girl having complete alopecia and nail dystrophy since birth. The family clearly showed linkage to chromosome 12q13.13-12q14.3, which excluded the KRT85 gene. Sequencing of another candidate gene HOXC13 within the linkage interval identified a homozygous frameshift mutation (c.355delC; p.Leu119Trpfs*20). Expression studies in cultured cells revealed that the mutant HOXC13 protein mislocalized within the cytoplasm, and failed to upregulate the promoter activities of its target genes. Our results strongly suggest crucial roles of the HOXC13 gene in the development of hair and nails in humans. In this study, we analyzed a consanguineous Syrian family with an affected girl with pure hair and nail ectodermal dysplasia, which is a rare genetic disorder characterized by alopecia and nail dystrophy since birth. Linkage studies and direct sequencing analysis led to the identification of a homozygous frameshift mutation (c.355delC; p.Leu119Trpfs*20) in the HOXC13 gene of the patient. In vitro studies in cultured cells demonstrated loss of function of the mutant HOXC13 protein. © 2013 Wiley Periodicals, Inc.