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New radiological finding by magnetic resonance imaging examination of the brain in Coffin-Lowry syndrome.

Authors :
Kondoh T
Matsumoto T
Ochi M
Sukegawa K
Tsuji Y
Source :
Journal of human genetics [J Hum Genet] 1998; Vol. 43 (1), pp. 59-61.
Publication Year :
1998

Abstract

We used magnetic resonance imaging (MRI) to examine the brain of a typical Coffin-Lowry syndrome (CLS) patient. There were many small perivascular focal areas of hypointensity in the white matter on T1-weighted images, similar to those found in mucopolysaccharidosis or perivascular leukomalacia. However, these changes could not seen in another patient we examined. Both patients showed normal urinary mucopolysaccharide patterns with chromatographic analysis. The cause of the MRI result is not known, but it could have a heterogeneous origin, and this result could represent an important indication defining one type of CLS.

Details

Language :
English
ISSN :
1434-5161
Volume :
43
Issue :
1
Database :
MEDLINE
Journal :
Journal of human genetics
Publication Type :
Academic Journal
Accession number :
9610000
Full Text :
https://doi.org/10.1007/s100380050038