Jaeger, E., Leedham, S., Lewis, A., Segditsas, S., Becker, M., Cuadrado, P.R., Davis, H., Kaur, K., Heinimann, K., Howarth, K., East, J., Taylor, J., Thomas, H. and Tomlinson, I. (2012) Hereditary mixed polyposis syndrome is caused by a 40-kb upstream duplication that leads to increased and ectopic expression of the BMP antagonist GREM1. Nature Genetics, 44, 699-703. doi:10.1038/ng.2263

has been cited by the following article:

• TITLE: Young patient with juvenile polyposis syndrome: A case report

  AUTHORS: Mounia El Yousfi, Bahija Benyachou, Adil Ibrahimi, Laila Chbani, Afaf Amarti

  KEYWORDS: Hamartomatous Polyp; Polyposis; Juvenile Polyp; Juvenile Polyposis

  JOURNAL NAME: Open Journal of Gastroenterology, Vol.2 No.3, August 30, 2012

  ABSTRACT: A case is reported here of juvenile polyposis in a 15- year-old girl. She was diagnosed upon the assessment of the dysenteric syndrome. Coloscopy and gastro- scopy had shown polyps of variable size whose histological study confirmed the hamartomatous character typical of the youthful non adenomatous polyps free of dysplasia. There was no localization in the small bowel. Coloprotectomy with ileoanal anastomosis was carried out in view of the importance of diarrhoea and the impacts on the general state of health.