Open Access Case report

A novel mitochondrial DNA deletion in a patient with Kearns-Sayre syndrome: a late-onset of the fatal cardiac conduction deficit and cardiomyopathy accompanying long-term rGH treatment

Monika Obara-Moszynska*, Jaroslaw Maceluch, Waldemar Bobkowski, Artur Baszko, Oskar Jaremba, Maciej R Krawczynski and Marek Niedziela

BMC Pediatrics 2013, 13:27  doi:10.1186/1471-2431-13-27

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