Congenital Coarctation of the Aorta in a Patient With ROBO4 c.695C>T (p.Thr232Met) Germline Variant

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Authors: Mohammad Karam Chaaban, George Bcharah, Bukola A. Olarewaju, Linnea M. Baudhuin, Fadi Elias Shamoun, Mayowa A. Osundiji
Cited by: 0
References: 14

Abstract

Roundabout guidance receptor 4 (ROBO4) germline variants [including c.695C>T (p.Thr232Met)] have been linked with bicuspid aortic valve and thoracic aortic aneurysm. However, the precise nature of ROBO4’s role in aortopathy is yet to be fully defined. We studied a 64-year-old woman with a history of surgically corrected congenital aortic coarctation in childhood, bicuspid aortic valve, and mild mitral regurgitation. She had genome sequencing, which revealed a heterozygous germline ROBO4 variant [c.695C>T (p.Thr232Met)]. Our findings suggest that the spectrum of aortic abnormalities that are associated with ROBO4 germline variants may include congenital coarctation of the aorta.

Fields of Study & Subjects

Congenital Heart Disease Studies Congenital heart defects research Cardiovascular Conditions and Treatments

Publication details

Journal / source
Annals of Internal Medicine Clinical Cases
Volume
5
Issue
1
Publication date
1 January 2026
Language
EN