SMAD4 mutation and the combined juvenile polyposis and hereditary hemorrhage telangiectasia syndrome: a single center experience

ConclusionsPatients with the combined JP –HHT syndrome remain at risk for life-threatening vascular complications and gastrointestinal malignancies; close follow-up is necessary to minimize morbidity and mortality in this patient population.

http://link.springer.com/10.1007/s00384-020-03670-3

Source: International Journal of Colorectal Disease - June 14, 2020 Category: Gastroenterology Source Type: research