Hostname: page-component-586b7cd67f-vdxz6 Total loading time: 0 Render date: 2024-11-24T21:31:36.734Z Has data issue: false hasContentIssue false

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

Image of the first page of this content. For PDF version, please use the ‘Save PDF’ preceeding this image.'
Type
Article Commentary
Copyright
© Cambridge University Press 2014 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

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