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Peutz-Jeghers syndrome

An inherited gastrointestinal disorder characterized by development of characteristic hamartomatous polyps throughout the gastrointestinal (GI) tract, and by mucocutaneous pigmentation. This disorder carries a considerably increased risk of GI and extra-GI malignancies.

Iron deficiency anemia

Total: 2

(per page)

PMID (PMCID)
14593545	FEMALE
	A Peutz-Jeghers syndrome case with iron deficiency anemia and jejuno-jejunal invagination.
	Sokmen HM, Ince AT, Bolukbas C, Kilic G, Dalay R, Kurdas OO. Turk J Gastroenterol. 2003;14(1):78-82.
	A Peutz-Jeghers syndrome case with iron deficiency anemia and jejuno-jejunal invagination.
7639241	MALE	Adult
	A case of Peutz-Jeghers syndrome with nasal polyposis, extreme iron deficiency anemia, and hamartoma-adenoma transformation: management by combined surgical and endoscopic approach.
	De Facq L, De Sutter J, De Man M, Van der Spek P, Lepoutre L. Am J Gastroenterol. 1995;90(8):1330-2.
	A case of Peutz-Jeghers syndrome with nasal polyposis, extreme iron deficiency anemia, and hamartoma-adenoma transformation: management by combined surgical and endoscopic approach.