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Gastrocutaneous syndrome

From Wikipedia, the free encyclopedia
Gastrocutaneous syndrome
Other namesPeptic ulcer/hiatal hernia, multiple lentigines/cafe-au-lait spots, hypertelorism, myopia[1]
Gastrocutaneous syndrome is an autosomal dominant disorder.
SpecialtyDermatology

Gastrocutaneous syndrome is a rare autosomal dominant cutaneous condition characterized by multiple lentigines.[2]

See also

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References

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  1. ^ "Gastrocutaneous syndrome | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. Retrieved 17 March 2019.
  2. ^ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 978-1-4160-2999-1.
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