Late onset asymptomatic pancreatic neuroendocrine tumor – A case report on the phenotypic expansion for MEN1

BACKGROUND: Multiple endocrine neoplasia type 1 (MEN1) is a hereditary cancer syndrome associated with several endocrine as well as non-endocrine tumors and is caused by mutations in the MEN1 gene. Primary hyperparathyroidism affects the majority of MEN1 individuals by age 50 years. Additionally, ME...

Full beskrivning

Sparad:
Bibliografiska uppgifter
I publikationen:Hered Cancer Clin Pract
Huvudupphovsmän: Kaiwar, Charu, Macklin, Sarah K., Gass, Jennifer M., Jackson, Jessica, Klee, Eric W., Hines, Stephanie L., Stauffer, John A., Atwal, Paldeep S.
Materialtyp: Artigo
Språk:Inglês
Publicerad: BioMed Central 2017
Ämnen:
Case Report
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC5521080/
https://ncbi.nlm.nih.gov/pubmed/28736585
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13053-017-0070-0
Taggar: Lägg till en tagg
Inga taggar, Lägg till första taggen!

Liknande verk