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New radiological finding by magnetic resonance imaging examination of the brain in Coffin-Lowry syndrome.
- 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.
- Subjects :
- Abnormalities, Multiple genetics
Abnormalities, Multiple urine
Child
Craniofacial Abnormalities genetics
Craniofacial Abnormalities pathology
Glycosaminoglycans urine
Humans
Intellectual Disability genetics
Intellectual Disability pathology
Magnetic Resonance Imaging
Male
Syndrome
Abnormalities, Multiple pathology
Brain pathology
Subjects
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