Familial progressive hyper- and hypopigmentation: a report on a Chinese family and evidence for genetic heterogeneity

BACKGROUND: Familial progressive hyper- and hypopigmentation (FPHH) is a rare genodermatosis that is characterized by diffuse hyper- and hypopigmented spots on the skin and mucous membranes. It is caused by a pathogenic mutation of the KITLG gene. OBJECTIVES: To investigate the clinical features and...

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Detalles Bibliográficos
Autores principales: Xiao-Kai, Fang, Yue-Xi, He, Yan-Jia, Li, Li-Rong, Chen, He-Peng, Wang, Qing, Sun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Dermatologia 2017
Materias:
Investigation
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5514571/
https://www.ncbi.nlm.nih.gov/pubmed/29186243
http://dx.doi.org/10.1590/abd1806-4841.20175567

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5514571/
https://www.ncbi.nlm.nih.gov/pubmed/29186243
http://dx.doi.org/10.1590/abd1806-4841.20175567

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