Gastrocutaneous syndrome is a rare autosomal dominant cutaneous condition characterized by multiple lentigines.[2]
Gastrocutaneous syndrome | |
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Other names | Peptic ulcer/hiatal hernia, multiple lentigines/cafe-au-lait spots, hypertelorism, myopia[1] |
Gastrocutaneous syndrome is an autosomal dominant disorder. | |
Specialty | Dermatology |
See also
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edit- ^ "Gastrocutaneous syndrome | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. Retrieved 17 March 2019.
- ^ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 978-1-4160-2999-1.
External links
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