Literature DB >> 28297138

A Novel Homozygous Missense Mutation in HOXC13 Leads to Autosomal Recessive Pure Hair and Nail Ectodermal Dysplasia.

Xiaoxiao Li1, Meredith Lee Orseth1, J Michael Smith1, Mary Abigail Brehm1, Nnenna Gebechi Agim1, Donald Alexander Glass1.   

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.
© 2017 Wiley Periodicals, Inc.

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Year:  2017        PMID: 28297138     DOI: 10.1111/pde.13074

Source DB:  PubMed          Journal:  Pediatr Dermatol        ISSN: 0736-8046            Impact factor:   1.588


  1 in total

1.  The inconsistent regulation of HOXC13 on different keratins and the regulation mechanism on HOXC13 in cashmere goat (Capra hircus).

Authors:  Shanhe Wang; Zhixin Luo; Yuelang Zhang; Dan Yuan; Wei Ge; Xin Wang
Journal:  BMC Genomics       Date:  2018-08-23       Impact factor: 3.969

  1 in total

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