Gastrocutaneous syndrome: Difference between revisions
From WikiMD's Wellness Encyclopedia
No edit summary Tag: visualeditor-wikitext |
CSV import |
||
| Line 15: | Line 15: | ||
{{Dermatology-stub}} | {{Dermatology-stub}} | ||
<gallery> | |||
File:Autosomal_dominant_-_en.svg | |||
</gallery> | |||
Revision as of 22:12, 16 February 2025
Gastrocutaneous syndrome is a rare autosomal dominant cutaneous condition characterized by multiple lentigines.
Other names
Peptic ulcer/hiatal hernia, multiple lentigines/cafe-au-lait spots, hypertelorism, myopia
Pathophysiology
It is a rare, syndromic, hyperpigmentation of the skin characterized by multiple lentigines and café-au-lait spots associated with hiatal hernia and peptic ulcer, hypertelorism and myopia.
See also

This article is a dermatology stub. You can help WikiMD by expanding it!