Atypical presentation of dyschromatosis universalis hereditaria with a novel ABCB6 mutation

Clin Exp Dermatol. 2019 Apr;44(3):e58-e60. doi: 10.1111/ced.13833. Epub 2018 Nov 14.

Authors

W Zhong^{1

2}, Y Pan^{1

2}, Y Shao³, Y Yang^{1

2

4}, B Yu³, Z Lin^{1

2}

Affiliations

¹ Department of Dermatology, Peking University First Hospital, Beijing, 100034, China.
² Beijing Key Laboratory of Molecular Diagnosis on Dermatoses, Beijing, China.
³ Department of Dermatology, Peking University Shenzhen Hospital, Shenzhen, Guangdong, 518036, China.
⁴ Peking-Tsinghua Center for Life Sciences, Beijing, 100871, China.

PMID: 30430618
DOI: 10.1111/ced.13833

No abstract available

Publication types

Case Reports
Letter
Research Support, Non-U.S. Gov't

MeSH terms

ATP-Binding Cassette Transporters / genetics*
Female
Humans
Male
Mutation
Pedigree
Phenotype
Pigmentation Disorders / congenital*
Pigmentation Disorders / genetics
Pigmentation Disorders / pathology
Skin Diseases, Genetic / genetics*
Skin Diseases, Genetic / pathology
Young Adult

Substances

ABCB6 protein, human
ATP-Binding Cassette Transporters

Supplementary concepts

Dyschromatosis universalis hereditaria

Grants and funding