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Cardiac anomalies in Axenfeld–Rieger syndrome

Published online by Cambridge University Press:  22 December 2022

Nishma Valikodath Open the ORCID record for Nishma Valikodath [Opens in a new window] ,
James A. Johns  and
Justin Godown
Nishma Valikodath*
Affiliation:
Department of Pediatrics, Monroe Carell Jr. Children’s Hospital at Vanderbilt, Nashville, USA
James A. Johns
Affiliation:
Division of Pediatric Cardiology, Monroe Carell Jr. Children’s Hospital at Vanderbilt, Nashville, USA
Justin Godown
Affiliation:
Division of Pediatric Cardiology, Monroe Carell Jr. Children’s Hospital at Vanderbilt, Nashville, USA
*
Author for correspondence: Nishma Valikodath, Department of Pediatrics, Monroe Carell Jr. Children’s Hospital, 2200 Children’s Way, DOT 8161, Nashville, TN 37232, USA. Tel: +1 615 936 2555. E-mail: nishma.valikodath@vumc.org
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Abstract

Axenfeld–Rieger syndrome is a rare multi-system disorder associated with cardiac anomalies. All patients with a diagnosis of Axenfeld–Rieger syndrome were identified from our electronic medical record. Chart review was performed to document the presence and types of CHD. Out of 58 patients, 14 (24.1%) had CHD and a wide variety of cardiac lesions were identified.

Keywords

Axenfeld–Rieger syndromeCHDglaucoma
Type
Brief Report
Information
Cardiology in the Young , Volume 33 , Issue 7 , July 2023 , pp. 1229 - 1231
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Copyright
© The Author(s), 2022. Published by Cambridge University Press

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