1. A recurrent mutation of GJB6 in a big Chinese family with Hidrotic ectodermal dysplasia
- Author
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Shuaihantian Luo, Guiying Zhang, Zixin Pi, and Yi Zhan
- Subjects
Adult ,Male ,0106 biological sciences ,China ,Ectodermal dysplasia ,medicine.medical_specialty ,lcsh:QH426-470 ,Prenatal diagnosis ,Gene mutation ,01 natural sciences ,03 medical and health sciences ,GJB6 ,Ectodermal Dysplasia ,Connexin 30 ,Genetics ,medicine ,Humans ,Missense mutation ,Genetic Predisposition to Disease ,Recurrent mutation ,Chinese family ,Gene ,Alleles ,Genetic Association Studies ,030304 developmental biology ,0303 health sciences ,biology ,Brief Report ,Sequence analysis ,Hidrotic ectodermal dysplasia ,Sequence Analysis, DNA ,General Medicine ,medicine.disease ,Dermatology ,Pedigree ,lcsh:Genetics ,Phenotype ,Mutation ,Gene mutations ,biology.protein ,Female ,010606 plant biology & botany - Abstract
Hidrotic ectodermal dysplasia (HED) is a rare inherited syndrome characterised by nail dystrophy, palmoplantar hyperkeratosis and alopecia. Four mutations (p.G11R, p.A88V, p.V37E and p.D50N) in gap junction beta 6 (GJB6) gene, which codes connexin30 protein, have been found to cause HED in different populations. Here, we reported a big Chinese family in which 24 patients over five generations were suffered with HED. Sequence analysis identified all 24 patients carry a recurrent missense mutation c.263C > T (p.A88V) in GJB6. Our results reveal gene testing of GJB6 is important for diagnosis, prenatal diagnosis and future gene treatment of HED.
- Published
- 2020
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