Abstract
We describe three cases of the rare syndrome of leukoencephalopathy, brain calcifications, and cysts. Conventional MRI, proton spectroscopy, and diffusion-weighted imaging yielded additional information on the disease. Imaging findings favor increased water content rather than a demyelinating process in the pathophysiology of this disease. Clinical features of Coats disease and consanguinity were also encountered.
Original language | English (US) |
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Pages (from-to) | 1206-1209 |
Number of pages | 4 |
Journal | Neurology |
Volume | 62 |
Issue number | 7 |
DOIs | |
State | Published - Apr 13 2004 |
ASJC Scopus subject areas
- Clinical Neurology