• 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