| Literature DB >> 17196380 |
L Boughamoura1, F Chaabane, S Tilouche, I Chabchoub, N Kabachi, K Tlili, M Yacoub, A-S Essoussi.
Abstract
Canavan disease or N-acetyl aspartic aciduria, is an autosomal recessive leukodystrophy characterized by spongy degeneration of brain. The disease is an inborn error of metabolism caused by aspartoacylase deficiency resulting from accumulation of N-acetyl aspartic acid in the brain. The authors report a case in a 10-month-old boy who presented with developmental delay and megalencephaly noticeable after 4 months of age. Magnetic resonance imaging of the brain showed diffuse white matter degeneration. The diagnosis of Canavan disease was confirmed by nuclear magnetic resonance spectroscopy and gas chromatography-mass spectrometry.Entities:
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Year: 2006 PMID: 17196380 DOI: 10.1016/j.arcped.2006.10.021
Source DB: PubMed Journal: Arch Pediatr ISSN: 0929-693X Impact factor: 1.180