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Implications of non-compaction in association with respiratory chain complex-I deficiency

Published online by Cambridge University Press:  18 November 2014

Josef Finsterer*
Affiliation:
Neurological Department, Krankenanstalt Rudolfstiftung, Vienna, Austria
Sinda Zarrouk-Mahjoub
Affiliation:
Laboratory of Biochemistry, UR Human Nutrition and Metabolic Disorders, Faculty of Medicine, Monastir, Tunisie
*
Correspondence to: Dr J. Finsterer, Postfach 20, 1180 Vienna, Austria, Europe. Tel: +431711 659 2085; Fax: +431 478 1711; E-mail: [email protected]

Abstract

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Type
Article Commentary
Copyright
© Cambridge University Press 2014 

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References

1. Dhar, R, Reardon, W, McMahon, CJ. Biventricular non-compaction hypertrophic cardiomyopathy in association with congenital complete heart block and type I mitochondrial complex deficiency. Cardiol Young 2014; 15: 13.Google Scholar
2. Finsterer, J, Stöllberger, C, Blazek, G, Sehnal, E. Familal left ventricular hypertrabeculation (noncompaction) is myopathic. Int J Cardiol 2013; 164: 312317.CrossRefGoogle ScholarPubMed
3. Correia, E, Rodrigues, B, Santos, L, et al. Noncompaction of the ventricular myocardium: characterization and follow-up of an affected population. Rev Port Cardiol 2011; 30: 323331.Google ScholarPubMed
4. Kirby, DM, Crawford, M, Cleary, MA, Dahl, HH, Dennett, X, Thorburn, DR. Respiratory chain complex I deficiency: an underdiagnosed energy generation disorder. Neurology 1999; 52: 12551264.CrossRefGoogle ScholarPubMed
5. Scaglia, F, Towbin, JA, Craigen, WJ, et al. Clinical spectrum, morbidity, and mortality in 113 pediatric patients with mitochondrial disease. Pediatrics 2004; 114: 925931.CrossRefGoogle ScholarPubMed
6. 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: 153158.CrossRefGoogle ScholarPubMed