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 ,
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