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Isolated aneurysmal disease as an underestimated finding in individuals with JAG1 pathogenic variants.

Authors :
Rodrigues Bento J
Krebsová A
Van Gucht I
Valdivia Callejon I
Van Berendoncks A
Votypka P
Luyckx I
Peldova P
Laga S
Havelka M
Van Laer L
Trunecka P
Boeckx N
Verstraeten A
Macek M
Meester JAN
Loeys B
Source :
Human mutation [Hum Mutat] 2022 Dec; Vol. 43 (12), pp. 1824-1828. Date of Electronic Publication: 2022 Jul 16.
Publication Year :
2022

Abstract

Pathogenic variants in JAG1 are known to cause Alagille syndrome (ALGS), a disorder that primarily affects the liver, lung, kidney, and skeleton. Whereas cardiac symptoms are also frequently observed in ALGS, thoracic aortic aneurysms have only been reported sporadically in postmortem autopsies. We here report two families with segregating JAG1 variants that present with isolated aneurysmal disease, as well as the first histological evaluation of aortic aneurysm tissue of a JAG1 variant carrier. Our observations shed more light on the pathomechanisms behind aneurysm formation in JAG1 variant harboring individuals and underline the importance of cardiovascular imaging in the clinical follow-up of such individuals.<br /> (© 2022 The Authors. Human Mutation published by Wiley Periodicals LLC.)

Details

Language :
English
ISSN :
1098-1004
Volume :
43
Issue :
12
Database :
MEDLINE
Journal :
Human mutation
Publication Type :
Academic Journal
Accession number :
35819173
Full Text :
https://doi.org/10.1002/humu.24433