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

• Autores principales: Jianbo Wang (Autor), Weisheng Li (Autor), Naihui Zhou (Autor), Jingliu Liu (Autor), Shoumin Zhang (Autor), Xueli Li (Autor), Zhenlu Li (Autor), Ziliang Yang (Autor), Miao Sun (Autor), Min Li (Autor)
• Formato: Libro
• Publicado: BMC, 2021-01-01T00:00:00Z.
• Materias: article
• Acceso en línea: 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...