Literature DB >> 3996146

Colorectal cancer in a nuclear family. Familial or hereditary?

H T Lynch, R Fitzgibbons, J Marcus, J McGill, G J Voorhees, J F Lynch.   

Abstract

Because of the high incidence of colorectal cancer, familial aggregations of this disease are common. Differentiation between etiologies contributing to familial clustering (which may have resulted either from common environmental exposure or from mere chance) and primary genetic factors may prove vexing to the physician. This report deals with the myriad problems encountered when attempting to make such etiologic distinctions in order to provide appropriate surveillance and management, based upon tumor spectrum and natural history, for patients at increased cancer risk.

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Year:  1985        PMID: 3996146     DOI: 10.1007/bf02560430

Source DB:  PubMed          Journal:  Dis Colon Rectum        ISSN: 0012-3706            Impact factor:   4.585


  2 in total

1.  Recognition and treatment of patients with hereditary nonpolyposis colon cancer (Lynch syndromes I and II).

Authors:  R J Fitzgibbons; H T Lynch; G V Stanislav; P A Watson; S J Lanspa; J N Marcus; T Smyrk; M D Kriegler; J F Lynch
Journal:  Ann Surg       Date:  1987-09       Impact factor: 12.969

2.  Congenital hypertrophy of the retinal pigment epithelium and mandibular osteomata as markers in familial colorectal cancer.

Authors:  L M Hunt; M H Robinson; C E Hugkulstone; B Clarke; S A Vernon; R H Gregson; J D Hardcastle; N C Armitage
Journal:  Br J Cancer       Date:  1994-07       Impact factor: 7.640

  2 in total

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