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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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| Udgivet i: | An Bras Dermatol |
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| Main Authors: | , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Sociedade Brasileira de Dermatologia
2017
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5514571/ https://ncbi.nlm.nih.gov/pubmed/29186243 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1590/abd1806-4841.20175567 |
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