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Holt–Oram syndrome with aortopulmonary window – a rare association

Published online by Cambridge University Press:  14 October 2013

Sunil K. Srinivas ,
Vijayalakshmi I. Balekundri  and
Cholenahally N. Manjunath
Sunil K. Srinivas*
Affiliation:
Department of Cardiology, Sri Jayadeva Institute of Cardiovascular Sciences and Research, Bangalore, Karnataka, India
Vijayalakshmi I. Balekundri
Affiliation:
Department of Pediatric Cardiology, Sri Jayadeva Institute of Cardiovascular Sciences and Research, Bangalore, Karnataka, India
Cholenahally N. Manjunath
Affiliation:
Department of Cardiology, Sri Jayadeva Institute of Cardiovascular Sciences and Research, Bangalore, Karnataka, India
*
Correspondence to: Dr S. K. Srinivas, MD, Fellow, Department of Cardiology, Sri Jayadeva Institute of Cardiovascular Sciences and Research, Bangalore, Karnataka 560069, India. Tel: +91-80-26650031; Fax: +91-80-22977422; E-mail: [email protected]
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Abstract

A 4-month-old male infant presented with recurrent cough for 2 months. He had a shortened right upper limb with absent right thumb and continuous murmur in the left parasternal area. The X-ray showed an absent radius and the first metacarpal and phalyngeal bones on the right side. Echocardiogram revealed aortopulmonary window and small secundum atrial septal defect. Aortopulmonary window was successfully treated by device closure. Holt–Oram syndrome with aortopulmonary window is an extremely rare association.

Keywords

Holt–Oram syndromeaortopulmonary windowatrial septal defect
Type
Brief Reports
Information
Cardiology in the Young , Volume 24 , Issue 5 , October 2014 , pp. 947 - 949
Copyright
Copyright © Cambridge University Press 2013 

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