Identification of a novel mutation in the KITLG gene in a Chinese family with familial progressive hyper- and hypopigmentation

• Main Authors: Jianbo Wang (Author), Weisheng Li (Author), Naihui Zhou (Author), Jingliu Liu (Author), Shoumin Zhang (Author), Xueli Li (Author), Zhenlu Li (Author), Ziliang Yang (Author), Miao Sun (Author), Min Li (Author)
• Format: Book
• Published: BMC, 2021-01-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Abstract Background Familial progressive hyper- and hypopigmentation (FPHH, MIM 145250) is a rare hereditary skin disorder that is predominantly characterized by progressive, diffuse, partly blotchy hyperpigmented lesions intermingled with scattered hypopigmented spots, lentigines and sometimes Cafe...