Back to Search Start Over

Molecular defects in Sanfilippo syndrome type B (mucopolysaccharidosis IIIB).

Authors :
Beesley CE
Jackson M
Young EP
Vellodi A
Winchester BG
Source :
Journal of inherited metabolic disease [J Inherit Metab Dis] 2005; Vol. 28 (5), pp. 759-67.
Publication Year :
2005

Abstract

Sanfilippo syndrome type B (mucopolysaccharidosis IIIB) is an autosomal recessive disease that is caused by the deficiency of the lysosomal enzyme alpha-N-acetylglucosaminidase (NAGLU). NAGLU is involved in the degradation of the glycosaminoglycan (GAG) heparan sulphate, and a deficiency results in the accumulation of partially degraded GAGs inside lysosomes. Early clinical symptoms include hyperactivity, aggressiveness and delayed development, followed by progressive mental deterioration, although there are a small number of late-onset attenuated cases. The gene for NAGLU has been fully characterized and we report the molecular analysis of 18 Sanfilippo B families. In total, 34 of the 36 mutant alleles were characterized in this study and 20 different mutations were identified including 8 novel changes (R38W, V77G, 407-410del4, 703delT, A246P, Y335C, 1487delT, E639X). The four novel missense mutations were transiently expressed in Chinese hamster ovary cells and all were shown to decrease the NAGLU activity markedly, although A246P did produce 12.7% residual enzyme activity.

Details

Language :
English
ISSN :
0141-8955
Volume :
28
Issue :
5
Database :
MEDLINE
Journal :
Journal of inherited metabolic disease
Publication Type :
Academic Journal
Accession number :
16151907
Full Text :
https://doi.org/10.1007/s10545-005-0093-y