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familial progressive hyperpigmentation (melanosis universalis hereditaria)
Genetics:
- autosomal-dominant
- associated with defects in KITLG
Clinical manifestations:
- hyperpigmented patches in the skin, present in early infancy, increasing in size & number with age
General
hyperpigmentation
genetic disease of the skin (genodermatosis)
Database Correlations
OMIM 145250
References
OMIM :accession 145250