Gastrocutaneous syndrome

From Wikipedia, the free encyclopedia
Jump to: navigation, search
Gastrocutaneous syndrome
Classification and external resources
OMIM 137270
MeSH C535651
Orphanet 2069

Gastrocutaneous syndrome is a rare autosomal dominant cutaneous condition characterized by multiple lentigines.[1]

See also[edit]

References[edit]

  1. ^ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 1-4160-2999-0.