Literature DB >> 21907889

Canavan disease: a novel mutation.

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.
Copyright © 2011 Elsevier Inc. All rights reserved.

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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


  2 in total

1.  Clinically Distinct Phenotypes of Canavan Disease Correlate with Residual Aspartoacylase Enzyme Activity.

Authors:  Marisa I Mendes; Desirée Ec Smith; Ana Pop; Pascal Lennertz; Matilde R Fernandez Ojeda; Warsha A Kanhai; Silvy Jm van Dooren; Yair Anikster; Ivo Barić; Caroline Boelen; Jaime Campistol; Lonneke de Boer; Ariana Kariminejad; Hulya Kayserili; Agathe Roubertie; Krijn T Verbruggen; Christine Vianey-Saban; Monique Williams; Gajja S Salomons
Journal:  Hum Mutat       Date:  2017-02-14       Impact factor: 4.878

2.  Problems of Unknown Significance: Counseling in the Era of Next Generation Sequencing.

Authors:  U Fahrioğlu
Journal:  Balkan J Med Genet       Date:  2018-10-29       Impact factor: 0.519

  2 in total

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