Results 61 to 70 of about 14,968 (77)

Familial juvenile adenomatous polyposis

Journal of Pediatric Surgery, 1976
Most colonic polyps in children are of the juvenile type and occur either as single or scattered colonic polyps. The peak incidence occurs between 4 and 6 yr of age, with a spontaneous decline from 12 to 15 yr. Significant clinical symptoms are rare, and operative therapy is rarely indicated.
F T, Velcek, I S, Coopersmith, C K, Chen, E G, Kassner, D H, Klotz, P K, kottmeier   +5 more
openaire   +2 more sources

Familial adenomatous polyposis

Cancer, 1997
BACKGROUND. Familial adenomatosis polyposis (FAP) is a prototype model for hereditary cancer. The adenomatous polyposis coli (APC) germline mutation, when identified within an FAP family, provides a powerful basis for early diagnosis. Indeed, the location of intragenic mutations in this large APC gene may distinguish the attenuated FAP variant ...
Henry T. Lynch, Susan T. Tinley, Jane Lynch, Jon Vanderhoof, Stephen J. Lemon   +4 more
openaire   +2 more sources

Familial Adenomatous Polyposis

Surgical Oncology Clinics of North America, 2007
Patients with FAP are guaranteed to have one major abdominal surgery in their life. They are also subject to cancers and benign disorders in other organ systems, some of which can be life threatening. Steering a course through life while avoiding preventable disease and complications of treatment, and maintaining good quality of life is a challenge for
openaire   +2 more sources

Familial Adenomatous Polyposis

Journal of the Royal Society of Medicine, 1992
Juan J. Nogueras, Steven D. Wexner, Patricia A. Brantley, David G. Jagelman, Ellen McGannon, James M. Church   +5 more
openaire   +3 more sources

FAMILIAL ADENOMATOUS POLYPOSIS

2005
Soravia, Claudio, Cohen, Z
openaire   +3 more sources

Familial adenomatous polyposis

Gastrointestinal Endoscopy, 2003
Marcia, Cruz-Correa, Francis M, Giardiello   +1 more
openaire   +2 more sources

Familial Adenomatous Polyposis

2002
Although the description of the first patient occurred more than 100 years ago, familial adenomatous polyposis (FAP or adenomatosis coli) continues to be the object of several convergent lines of scientific and medical interest. Familial gastrointestinal polyposis includes various rare syndromes with the common features of numerous polyps (often ...
openaire   +1 more source

[Familial adenomatous polyposis].

Ugeskrift for laeger, 1990
Familial adenomatous polyposis is a dominant hereditary disease which includes early development of up to several thousand colorectal adenomas and subsequent development of colorectal adenocarcinoma in all of the untreated cases. In addition, various extracolonic manifestations may be observed.
S, Bülow, J O, Søndergaard, F, Moesgaard   +2 more
openaire   +1 more source

Gastrointestinal: Familial adenomatous polyposis

Journal of Gastroenterology and Hepatology, 1998
D J, Moore, I C, Roberts-Thomson
openaire   +2 more sources

Familial adenomatous polyposis

Middle East Journal of Medical Genetics, 2014
Makia J. Marafie, Farah L. Al-Elwani, Ibrahim S. Al Suliman   +2 more
openaire   +1 more source