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Large- and medium-sized arterial aneurysms in two patients with SMAD4-related juvenile polyposis syndrome.

Authors :
van Weelden W
Bleeker FE
van Stijn D
Micha D
Maugeri A
Kuijpers TW
Koch AD
Aalfs CM
Wagner A
Groenink M
van Oldenrijk J
Baars MJ
Duijkers FAM
Source :
American journal of medical genetics. Part A [Am J Med Genet A] 2024 Oct; Vol. 194 (10), pp. e63605. Date of Electronic Publication: 2024 May 16.
Publication Year :
2024

Abstract

Germline SMAD4 pathogenic variants (PVs) cause juvenile polyposis syndrome (JPS), which is known for an increased risk of gastrointestinal juvenile polyps and gastrointestinal cancer. Many patients with SMAD4 PV also show signs of hereditary hemorrhagic telangiectasia (HHT) and some patients have aneurysms and dissections of the thoracic aorta. Here we describe two patients with a germline SMAD4 PV and a remarkable clinical presentation including multiple medium-sized arterial aneurysms. More data are needed to confirm whether the more extensive vascular phenotype and the other described features in our patients are indeed part of a broader JPS spectrum.<br /> (© 2024 The Authors. American Journal of Medical Genetics Part A published by Wiley Periodicals LLC.)

Details

Language :
English
ISSN :
1552-4833
Volume :
194
Issue :
10
Database :
MEDLINE
Journal :
American journal of medical genetics. Part A
Publication Type :
Academic Journal
Accession number :
38752492
Full Text :
https://doi.org/10.1002/ajmg.a.63605