Familial progressive hyper- and hypopigmentation and malignancy in two families with new mutations in KITLG.

Volume: 40, Issue: 8, Pages: 860 - 864
Published: Dec 1, 2015
Abstract
Background null Familial progressive hyper- and hypopigmentation (FPHH) is an autosomal dominant skin condition presenting in childhood with generalized macular dyspigmentation, usually reported in patients of East Asian origin. It overlaps phenotypically with other dyschromatoses, but can now be distinguished by mutations in the KIT ligand gene (KITLG). null Aim null We report two unrelated white families with similar phenotypic presentations...
Paper Details
Title
Familial progressive hyper- and hypopigmentation and malignancy in two families with new mutations in KITLG.
Published Date
Dec 1, 2015
Volume
40
Issue
8
Pages
860 - 864
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