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Response to commentary: biventricular non-compaction hypertrophic cardiomyopathy in association with congenital complete heart block and type I mitochondrial complex deficiency

Published online by Cambridge University Press:  01 June 2015

Ranjana Dhar ,
William Reardon  and
Colin J. McMahon
Ranjana Dhar
Affiliation:
Department of Paediatric Cardiology, Our Lady’s Hospital for Sick Children, Crumlin, Dublin, Ireland
William Reardon
Affiliation:
National Centre for Medical Genetics, Our Lady’s Hospital for Sick Children, Crumlin, Dublin, Ireland
Colin J. McMahon*
Affiliation:
Department of Paediatric Cardiology, Our Lady’s Hospital for Sick Children, Crumlin, Dublin, Ireland
*
Correspondence to: C. J. McMahon, Cardiac Department, Our Lady’s Hospital for Sick Children, Crumlin, Dublin 12, Ireland. Tel: +01 409 6160; Fax: +01 409 6181; E-mail: cmcmahon992004@yahoo.com
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Abstract

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Type
Commentary
Information
Cardiology in the Young , Volume 25 , Issue 5 , June 2015 , pp. 1024 - 1025
Copyright
© Cambridge University Press 2015 

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References

1. Dhar, R, Reardon, W, McMahon, CJ. Biventricular noncompaction hypertrophic cardiomyopathy in association with congenital complete heart block and type I mitochondrial complex deficiency. Cardiol Young 2014; 15: 1–3.Google Scholar
2. Finsterer, J, Zarrouk-Mahjoub, S. Implications of non-compaction in association with respiratory chain complex-1 deficiency. Cardiol Young 2014; 18: 1–2.Google Scholar
3. Scaglia, F, Towbin, JA, Criagen, WJ, et al. Clinical spectrum, morbidity, and mortality in 113 pediatric patients with mitochondrial disease. Pediatrics 2004; 114: 925–931.Google Scholar
4. Zarrouk Mahjoub, S, Mehri, S, Ourda, F, et al. Transition m.3308T>C in the ND1 gene is associated with left ventricular hypertrabeculation/noncompaction. Cardiology 2011; 118: 153–158.Google Scholar