| Literature DB >> 21907889 |
Harald Schober1, Juerg Luetschg, Isabella Hoeliner, Stefanie Kalb, Burkhard Simma.
Abstract
Canavan disease, an autosomal recessive inherited leukodystrophy caused by an aspartoacylase deficiency, is common among children of Ashkenazi Jewish descent. We report on a non-Jewish female infant who presented at age 6 months with progressive macrocephaly and developmental delay. A sequence analysis of the aspartoacylase gene revealed compound heterozygosity for a known mutation and for the mutation c.432G>A in exon 2, which has not yet been described in Canavan disease.Entities:
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Year: 2011 PMID: 21907889 DOI: 10.1016/j.pediatrneurol.2011.06.011
Source DB: PubMed Journal: Pediatr Neurol ISSN: 0887-8994 Impact factor: 3.372