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J Inherit Metab Dis. 2007 Jun;30(3):358-64. Epub 2007 Apr 24.

Bovine mucopolysaccharidosis type IIIB.

Author information

1
Lysosomal Diseases Research Unit, Department of Genetic Medicine, Children, Youth and Women's Health Service, 72 King William Road, North Adelaide, 5006, South Australia, Australia. litsa.karageorgos@cywhs.sa.gov.au

Abstract

Mucopolysaccharidosis IIIB, an autosomal recessive lysosomal storage disorder of heparan sulfate caused by mutations in the alpha-N-acetylglucosaminidase (NAGLU) gene, was recently discovered in cattle. Clinical signs include progressive ataxia, stumbling gait, swaying and difficulty in balance and walking. These clinical signs are usually first observed at approximately 2 years of age and then develop progressively over the lifespan of the animals. Affected bulls were found to be homozygous for the missense mutation E452K (c.1354G > A). The availability of mutational analysis permits screening for the NAGLU mutation to eradicate this mutation from the cattle breeding population.

PMID:
17458708
DOI:
10.1007/s10545-007-0539-5
[Indexed for MEDLINE]

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