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Canavan disease: findings in four new cases

✍ Scribed by H. Michelakakis; S. Giouroukos; P. Divry; E. Katsarou; M. O. Rolland; A. Skardoutsou

Publisher
Springer
Year
1991
Tongue
English
Weight
174 KB
Volume
14
Category
Article
ISSN
0141-8955

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## Abstract Two children with Canavan's Disease, an autosomal recessive leukodystrophy, were studied by localized ^1^H spectroscopy. The __N__‐acetylaspartate (NAA) signal intensity was high relative to other metabolite signals, and the signal intensity from choline‐containing compounds was low. Th