Medical Definition of Jeghers-Peutz syndrome
1.
Autosomal dominant (50% sporadic), hamartomas, primarily of small bowel, also: stomach, colon, occasionally of urinary or respiratory tract, mucocutaneous hyperpigmentation, increased risk of GI and non-GI tumours! (NEJM 1988) Cf: polyposis syndromes
(12 Dec 1998)
Lexicographical Neighbors of Jeghers-Peutz Syndrome
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