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[Hamartomatous polyposis syndromes].
Recenti Prog Med. 2004 Feb; 95(2):101-3.RP

Abstract

Hamartomatous polyposis syndromes are characterized by an overgrowth of cells or tissues native to the area in which they normally occur. Peutz-Jeghers syndrome and juvenile polyposis are both characterized by the presence of hamartomatous polyps and increased risk of malignancy in the gastrointestinal tract. Cowden's disease is associated with germ-line mutations in the PTEN gene (10q22-23) and an increased risk of breast and thyroid malignancies. Ruvalcaba-Myhre-Smith syndrome is less common; controversy suggests that it may represent a variant of Cowden's disease.

Authors

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Pub Type(s)

Editorial
English Abstract
Review

Language

ita

PubMed ID

15072395

Citation

Bossone, Giandominik, et al. "[Hamartomatous Polyposis Syndromes]." Recenti Progressi in Medicina, vol. 95, no. 2, 2004, pp. 101-3.
Bossone G, Salesi N, Alghisi F, et al. [Hamartomatous polyposis syndromes]. Recenti Prog Med. 2004;95(2):101-3.
Bossone, G., Salesi, N., Alghisi, F., & Di Cocco, B. (2004). [Hamartomatous polyposis syndromes]. Recenti Progressi in Medicina, 95(2), 101-3.
Bossone G, et al. [Hamartomatous Polyposis Syndromes]. Recenti Prog Med. 2004;95(2):101-3. PubMed PMID: 15072395.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - [Hamartomatous polyposis syndromes]. AU - Bossone,Giandominik, AU - Salesi,Nello, AU - Alghisi,Federico, AU - Di Cocco,Barbara, PY - 2004/4/10/pubmed PY - 2005/1/5/medline PY - 2004/4/10/entrez SP - 101 EP - 3 JF - Recenti progressi in medicina JO - Recenti Prog Med VL - 95 IS - 2 N2 - Hamartomatous polyposis syndromes are characterized by an overgrowth of cells or tissues native to the area in which they normally occur. Peutz-Jeghers syndrome and juvenile polyposis are both characterized by the presence of hamartomatous polyps and increased risk of malignancy in the gastrointestinal tract. Cowden's disease is associated with germ-line mutations in the PTEN gene (10q22-23) and an increased risk of breast and thyroid malignancies. Ruvalcaba-Myhre-Smith syndrome is less common; controversy suggests that it may represent a variant of Cowden's disease. SN - 0034-1193 UR - https://www.unboundmedicine.com/medline/citation/15072395/[Hamartomatous_polyposis_syndromes]_ DB - PRIME DP - Unbound Medicine ER -
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