Title of article :
Severe lactic acidosis secondary to minocycline in a teenager with infectious mononucleosis and mitochondrial myopathy
Author/Authors :
Richard M. Zoraster، نويسنده , , Richard A. Rison، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2008
Pages :
4
From page :
627
To page :
630
Abstract :
Mitochondrial myopathies are heterogeneous disorders with diverse presentations including laboratory findings of lactic acidosis. Often times they are diagnosed in childhood or the early teenage years following an infectious illness. Minocycline is a common antibiotic used for the treatment of acne. It has been reported to alter mitochondrial respiratory chain complexes. We report an interesting case of a teenager in which mitochondrial myopathy with severe lactic acidosis presented following a bout of infectious mononucleosis and minocycline use. It is hypothesized that oxidative stress from the infectious illness plus the minocycline use triggered the patientʹs presentation. The clinical manifestations and genetics of mitochondrial myopathies and treatment are discussed along with the management of lactic acidosis.
Keywords :
Infectious mononucleosis , Lactic acidosis , Mitochondrial myopathy , Minocycline , G8363A mutation , Ribosome inhibitor , Respiratory chaincomplexes
Journal title :
Clinical Neurology and Neurosurgery
Serial Year :
2008
Journal title :
Clinical Neurology and Neurosurgery
Record number :
464666
Link To Document :
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