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.

Obara-Moszynska, Monika

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. [electronic resource] - BMC pediatrics Feb 2013 - 27 p. digital

Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

1471-2431

10.1186/1471-2431-13-27 doi


Adolescent
Atrioventricular Block--diagnosis
Base Sequence
Cardiomyopathy, Dilated--diagnosis
DNA, Mitochondrial
Fatal Outcome
Growth Disorders--drug therapy
Human Growth Hormone--deficiency
Humans
Kearns-Sayre Syndrome--complications
Male
Recombinant Proteins
Sequence Deletion