Canavan Disease: CT and MR Imaging of the Brain
Overview
Affiliations
Canavan disease (spongy degeneration of the brain) is a rare lethal neurodegenerative disorder of infancy; fewer than 100 cases have been reported. We describe a series of nine patients with enzymatic defects and clinical features consistent with Canavan disease; in two patients the disease was proved by biopsy. All patients were examined with CT and seven with MR. In every instance, both CT and MR showed white-matter disease, sometimes sparing the external and internal capsules, the corpus callosum, and the deep cerebellar white matter. Atrophic changes were found in six patients; the changes were marked in one and slight in five. There was no obvious correlation between the severity of the white-matter disease and the clinical presentation--one patient with severe white-matter disease was clinically normal. The CT and MR findings in Canavan disease are nonspecific and somewhat nonuniform: its preautopsy diagnosis relies primarily on biochemical findings.
Isasi E, Wajner M, Duarte J, Olivera-Bravo S Neurotox Res. 2024; 42(4):33.
PMID: 38963434 DOI: 10.1007/s12640-024-00710-6.
Cellular and molecular mechanisms of aspartoacylase and its role in Canavan disease.
Gronbaek-Thygesen M, Hartmann-Petersen R Cell Biosci. 2024; 14(1):45.
PMID: 38582917 PMC: 10998430. DOI: 10.1186/s13578-024-01224-6.
Cribriform Appearance of White Matter in Canavan Disease Associated with Novel Mutations of Gene.
Bhat M, Manjunath N, Kumari R, Faruq M, Pal P, Prasad C J Pediatr Genet. 2022; 11(4):267-271.
PMID: 36267868 PMC: 9578778. DOI: 10.1055/s-0041-1725118.
The pathogenesis of, and pharmacological treatment for, Canavan disease.
Wei H, Moffett J, Amanat M, Fatemi A, Tsukamoto T, Namboodiri A Drug Discov Today. 2022; 27(9):2467-2483.
PMID: 35636725 PMC: 11806932. DOI: 10.1016/j.drudis.2022.05.019.
Diagnostic Approach to Macrocephaly in Children.
Accogli A, Geraldo A, Piccolo G, Riva A, Scala M, Balagura G Front Pediatr. 2022; 9:794069.
PMID: 35096710 PMC: 8795981. DOI: 10.3389/fped.2021.794069.