Medical Definition of Peutz-jeghers 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 Peutz-jeghers Syndrome
Other Resources:
