Familial Gastrointestinal Stromal Tumors and Germ-Line Mutations

  • McWhinney S
  • Pasini B
  • Stratakis C
210Citations
Citations of this article
67Readers
Mendeley users who have this article in their library.

Abstract

To the Editor: Gastrointestinal stromal tumors may be sporadic or inherited in an autosomal dominant manner, alone or as a component of a syndrome associated with other tumors, such as in the context of neurofibromatosis type 1.1 We have described seven male and five female patients (median age, 23 years) from five unrelated families who had both gastrointestinal stromal tumors and paragangliomas. Susceptibility to the tumors was inherited in an apparently autosomal dominant manner, with incomplete penetrance.2 This condition has been referred to as “the dyad of paraganglioma and gastrointestinal stromal tumors” or the “Carney–Stratakis syndrome” (or “Carney–Stratakis dyad”).3 Germ-line . . .

Cite

CITATION STYLE

APA

McWhinney, S. R., Pasini, B., & Stratakis, C. A. (2007). Familial Gastrointestinal Stromal Tumors and Germ-Line Mutations. New England Journal of Medicine, 357(10), 1054–1056. https://doi.org/10.1056/nejmc071191

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free