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Bovine mucopolysaccharidosis type IIIB.
- Source :
-
Journal of inherited metabolic disease [J Inherit Metab Dis] 2007 Jun; Vol. 30 (3), pp. 358-64. Date of Electronic Publication: 2007 Apr 24. - Publication Year :
- 2007
-
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.
- Subjects :
- Animals
Brain pathology
Cattle
Cattle Diseases enzymology
Cattle Diseases pathology
DNA genetics
DNA isolation & purification
Genome
Mucopolysaccharidosis III enzymology
Mucopolysaccharidosis III genetics
Mucopolysaccharidosis III pathology
Neurons pathology
Neurons ultrastructure
Reference Values
Skin chemistry
Thalamic Nuclei pathology
Acetylglucosaminidase genetics
Cattle Diseases genetics
Mucopolysaccharidosis III veterinary
Mutation, Missense
Subjects
Details
- Language :
- English
- ISSN :
- 1573-2665
- Volume :
- 30
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Journal of inherited metabolic disease
- Publication Type :
- Academic Journal
- Accession number :
- 17458708
- Full Text :
- https://doi.org/10.1007/s10545-007-0539-5