SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature
June 2025
in “
Pigment Cell & Melanoma Research
”
Studysummary This literature review reports that mutations in the SASH1 gene are linked to different pigmentation disorders, including dyschromatosis universalis hereditaria and lentiginosis. It further suggests SASH1's significant role in melanocyte processes and its potential as a target for developing treatments for these conditions.
Our plain-language summary. Not medical advice or a treatment recommendation. Consult a qualified healthcare professional before changing treatment. Full disclaimer