A novel mutation in ABCB6 associated with dyschromatosis universalis hereditaria in a Saudi family

JAAD Case Rep. 2021 Nov 25:19:97-99. doi: 10.1016/j.jdcr.2021.11.017. eCollection 2022 Jan.

Authors

Sara Aldokhayel¹, Alballa Nouf¹, Aleedan Khalid², Alsaif Faisal², Alotaibi Maram³, Alhumidi Ahmed⁴, Alsaif Fahad¹

Affiliations

¹ Department of Dermatology, Riyadh, Saudi Arabia.
² College of Medicine, Riyadh, Saudi Arabia.
³ Department of Genetics, Riyadh, Saudi Arabia.
⁴ Department of Pathology, College of Medicine, King Saud University, Riyadh, Saudi Arabia.

No abstract available

Keywords: DUH, dychromatosis universalis heredetaria; dyschromatosis; genetic diseases; hyperpigmented; hypopigmented; melanosomes.

Publication types

Case Reports