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)|
|Number of pages||4|
|State||Published - Apr 13 2004|
ASJC Scopus subject areas
- Clinical Neurology