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Mitochondrial encephalocardio-myopathy with early neonatal onset due to TMEM70 mutation

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    0355558 - FGÚ 2011 RIV GB eng J - Journal Article
    Honzík, T. - Tesařová, M. - Mayr, J. A. - Hansíková, H. - Ješina, P. - Bodamer, O. - Koch, J. - Magner, M. - Freisinger, P. - Huemer, M. - Kostková, O. - Van Coster, R. - Kmoch, S. - Houštěk, Josef - Sperl, W. - Zeman, J.
    Mitochondrial encephalocardio-myopathy with early neonatal onset due to TMEM70 mutation.
    Archives of Disease in Childhood. Roč. 95, č. 4 (2010), s. 296-301. ISSN 0003-9888. E-ISSN 1468-2044
    R&D Projects: GA MZd(CZ) NS9759; GA MŠMT(CZ) 1M0520
    Institutional research plan: CEZ:AV0Z50110509
    Keywords : TMEM70 * ATP synthase * mitochondrial disease
    Subject RIV: FG - Pediatrics
    Impact factor: 2.616, year: 2010

    Multi-site survey characterization of a natural course of a novel mitochondrial disease. ATP synthase deficiency with mutation in TMEM70 should be considered in diagnostics and management of critically ill neonates with early neonatal onset of muscular hypotonia, hypertrophic cardiomyopathy and hypospadias in boys accompanied with lactic acidosis, hyperammonemia and 3-methylglutaconic aciduria. However, the severity of the phenotype may vary significantly. The disease occurs frequently in Roman population and molecular-genetic analysis of TMEM70 gene is sufficient for diagnostics without the need of muscle biopsy in affected children
    Permanent Link: http://hdl.handle.net/11104/0194302

     
     
Number of the records: 1  

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