Patient with Marfan syndrome and a novel variant in FBN1 presenting with bilateral popliteal artery aneurysm

Mohammad, A., Helmi, H. and Atwal, P. S. (2018) Patient with Marfan syndrome and a novel variant in FBN1 presenting with bilateral popliteal artery aneurysm. Case Reports in Genetics, 2018, 6780494. (doi: 10.1155/2018/6780494) (PMID:29796325) (PMCID:PMC5896231)

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Abstract

We present a 43-year-old man with aortic root dilation, mitral valve prolapse, and marfanoid appearance, who presented with acute onset left leg pain. He underwent a Doppler ultrasound that revealed left popliteal artery aneurysm with thrombus. CT angiogram showed bilateral popliteal artery aneurysms. After repairing of his left popliteal artery aneurysm, he was sent for genetic evaluation. He was diagnosed with Marfan syndrome (MFS) based on the revised Ghent criteria and then underwent FBN1 sequencing and deletion/duplication analysis, which detected a novel pathogenic variant in gene FBN1, denoted by c.5872 T>A (p.Cys1958Ser). MFS is a connective tissue disorder with an autosomal dominant inheritance due to pathogenic variants in FBN1 that encodes Fibrillin-1, a major element of the extracellular matrix, and connective tissue throughout the body. MFS involves multiple systems, most commonly the cardiovascular, musculoskeletal, and visual systems. In our case we present a rare finding of bilateral popliteal artery aneurysms in a male patient with MFS.

Item Type:Articles
Status:Published
Refereed:Yes
Glasgow Author(s) Enlighten ID:Atwal, Dr Paldeep
Authors: Mohammad, A., Helmi, H., and Atwal, P. S.
College/School:College of Medical Veterinary and Life Sciences > School of Medicine, Dentistry & Nursing
Journal Name:Case Reports in Genetics
Publisher:Hindawi
ISSN:2090-6544
ISSN (Online):2090-6552
Published Online:29 March 2018
Copyright Holders:Copyright © 2018 Ahmed Mohammad et al.
First Published:First published in Case Reports in Genetics 2018: 6780494
Publisher Policy:Reproduced under a Creative Commons License

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