| Literature DB >> 12973663 |
M Bugiani1, I Moroni, A Bizzi, N Nardocci, T Bettecken, J Gärtner, G Uziel.
Abstract
Megalencephalic leukoencephalopathy with subcortical cysts (MLC) is a genetic disorder featuring diffuse MRI white matter abnormalities and a discrepantly mild clinical picture. It is related to different mutations in MLC1 gene encoding a putative membrane protein of still unknown function. We report on a genetically proven MLC patient who presented with a peculiar clinical course characterized by a prolonged comatose state following a minor head trauma at 12 years of age. The disturbance of consciousness lasted for over four months and then gradually improved. Proton MR spectroscopic imaging studies showed a moderately severe depletion of N-acetylaspartate restricted to the white matter with sparing of the cortical grey matter. The full recovery from coma suggests a transitory functional impairment of the structures implicated in the maintenance of consciousness.Entities:
Mesh:
Year: 2003 PMID: 12973663 DOI: 10.1055/s-2003-42209
Source DB: PubMed Journal: Neuropediatrics ISSN: 0174-304X Impact factor: 1.947