• Title of article

    Unusual magnetic resonance imaging features in Menkes disease

  • Author/Authors

    Christine Barnerias a، نويسنده , , Nathalie Boddaert b، نويسنده , , c، نويسنده , , Guiraud Pascale d، نويسنده , , Desguerre Isabelle a، نويسنده , , Lucie Hertz Pannier b، نويسنده , , e، نويسنده , , Olivier Dulac، نويسنده , , e، نويسنده , , Pascale de Lonlay a، نويسنده , , f، نويسنده , , Nadia Bahi Buisson a، نويسنده , , e، نويسنده , , *، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2008
  • Pages
    4
  • From page
    489
  • To page
    492
  • Abstract
    We present a case of an inherited disorder of copper metabolism, Menkes disease in which MRI studies revealed the coexistence of T2 hypersignal in the temporal white matter with an increase of apparent diffusion coefficient indicative of vasogenic oedema combined with T2 hypersignal of the putamen and head of the caudate and decreased apparent diffusion coefficient indicative of cytotoxic oedema. These unusual MRI features emphasize the interest of newly developed techniques in early diagnosis in Menkes disease. The acute cerebral damage might result from the combined effects of acute metabolic stress due to infectious disease and prolonged status epilepticus, acting on a highly susceptible developing brain. Vasogenic oedema in the temporal white matter could be related to prolonged status epilepticus and vascular abnormalities. Cytotoxic oedema of the putamen and head caudate could result from energetic failure.
  • Keywords
    Copper transport deficiency , Cytotoxic oedema , Menkes disease , Basal ganglia
  • Journal title
    Brain and Development
  • Serial Year
    2008
  • Journal title
    Brain and Development
  • Record number

    495262