Is colorectal surveillance indicated in patients with PTEN mutations?

Nieuwenhuis, M H; Kets, C M; Murphy-Ryan, M; Colas, C; Möller, P; Hes, F J; Hodgson, S V; Olderode-Berends, M J W; Aretz, S; Heinimann, K; Gomez Garcia, E B; Douglas, F; Spigelman, A; Timshel, S; Lindor, N M; Vasen, H F A

Nieuwenhuis, M H; Kets, C M; Murphy-Ryan, M; Colas, C; Möller, P; Hes, F J; Hodgson, S V; Olderode-Berends, M J W; Aretz, S; Heinimann, K; Gomez Garcia, E B; Douglas, F; Spigelman, A; Timshel, S; Lindor, N M; Vasen, H F A.

Affiliation

Nieuwenhuis MH; Netherlands Foundation for the Detection of Hereditary Tumors, Leiden, The Netherlands. m.nieuwenhuis@stoet.nl

Colorectal Dis ; 14(9): e562-6, 2012 Sep.

Article in En | MEDLINE | ID: mdl-22672595

Subject(s)

Colonic Polyps/genetics; Colorectal Neoplasms/genetics; Hamartoma Syndrome, Multiple/genetics; PTEN Phosphohydrolase/genetics; Adolescent; Adult; Aged; Child; Child, Preschool; Cohort Studies; Colonic Polyps/etiology; Colorectal Neoplasms/etiology; Female; Genetic Predisposition to Disease; Germ-Line Mutation; Hamartoma Syndrome, Multiple/complications; Humans; Infant; Kaplan-Meier Estimate; Male; Middle Aged

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hamartoma Syndrome, Multiple / Colorectal Neoplasms / Colonic Polyps / PTEN Phosphohydrolase Type of study: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies / Screening_studies Limits: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged Language: En Journal: Colorectal Dis Year: 2012 Document type: Article

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