[Juvenile polyposis syndrome is a rare cause of gastrointestinal cancer]

Ugeskr Laeger. 2014 Oct 27;176(44):V06130391.
[Article in Danish]

Abstract

Juvenile polyposis syndrome is an autosomal dominant polyposis syndrome. It is characterized by predisposition to multiple juvenile polyps in the gastrointestinal tract and is associated with an increased risk of colorectal and ventricular cancer. Patients and at risk family members should be offered surveillance. This article discusses clinical features and surveillance based on the current literature.

Publication types

  • Review

MeSH terms

  • Bone Morphogenetic Protein Receptors, Type I / genetics
  • Critical Pathways
  • Gastrointestinal Neoplasms / etiology*
  • Germ-Line Mutation
  • Humans
  • Intestinal Polyposis / complications*
  • Intestinal Polyposis / congenital
  • Intestinal Polyposis / diagnosis
  • Intestinal Polyposis / genetics
  • Neoplastic Syndromes, Hereditary / complications*
  • Neoplastic Syndromes, Hereditary / diagnosis
  • Neoplastic Syndromes, Hereditary / genetics
  • Neoplastic Syndromes, Hereditary / pathology
  • Risk Factors
  • Smad4 Protein / genetics
  • Telangiectasia, Hereditary Hemorrhagic / diagnosis
  • Telangiectasia, Hereditary Hemorrhagic / genetics

Substances

  • Smad4 Protein
  • BMPR1A protein, human
  • Bone Morphogenetic Protein Receptors, Type I