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
Link To Document :
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