Symptomatic anomalous right coronary artery in mother and daughter, a case report

Further reporting and genetic testing of patients with AORCA is warranted to evaluate heritability. This would allow for expedited diagnostic accuracy for patients with an unclear clinical presentation.

Authors

Chadi Nahal
Neil M. Borden
Eric Johnson
Cristiano Faber

Institutions

John F. Kennedy Medical Center (US)

Publication Details

Journal: Journal of Cardiothoracic Surgery
Published: 2025-10-29
DOI: https://doi.org/10.1186/s13019-025-03649-7
Primary Topic: Coronary Artery Anomalies
Type: article
Field-Weighted Citation Impact: 0.00

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article

Symptomatic anomalous right coronary artery in mother and daughter, a case report

Chadi Nahal, Neil M. Borden, Eric Johnson, Cristiano Faber

Oct 29, 2025

Journal of Cardiothoracic Surgery

Coronary Artery Anomalies

article

Symptomatic anomalous right coronary artery in mother and daughter, a case report

Chadi Nahal, Neil M. Borden, Eric Johnson, Cristiano Faber

October 29, 2025article en

Abstract

Journal of Cardiothoracic SurgeryVol. 20(1)

John F. Kennedy Medical Center (US)

Openalex Percentile: Top 55%

Coronary Artery Anomalies

DOI Open Access PDF OpenAlex

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Symptomatic anomalous right coronary artery in mother and daughter, a case report — Chadi Nahal, Neil M. Borden, et al. · Journal of Cardiothoracic Surgery (2025) | TGRS Research Map | TGRS