%0 Journal Article
%T Familial progressive hyper- and hypopigmentation: a report on a
Chinese family and evidence for genetic heterogeneity
%A Chen Li-Rong
%A Fang Xiao-Kai
%A He Yue-Xi
%A Sun Qing
%A Wang He-Peng
%J Archive of "Anais Brasileiros de Dermatologia".
%D 2017
%R 10.1590/abd1806-4841.20175567
%X 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
%K Genetic heterogeneity
%K Hyperpigmentation
%K Hypopigmentation
%K Immunohistochemistry
%K Mutation
%U https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5514571/