Literature DB >> 17196380

[Canavan disease or N-acetyl aspartic aciduria: a case report].

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.

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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


  1 in total

1.  Early diagnosis of Canavan syndrome: how can we get there?

Authors:  Giuseppe De Bernardo; Maurizio Giordano; Desiree Sordino; Salvatore Buono
Journal:  BMJ Case Rep       Date:  2015-08-05
  1 in total

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