Literature DB >> 6809360

Sanfilippo B syndrome (MPS III B): altered residual alpha-N-acetylglucosaminidase activity in an unusual sibship.

P Di Natale, P Murino, G Pontarelli, D Salvatore, G Andria.   

Abstract

We studied the residual alpha-N-acetylglucosaminidase activity in two siblings with severe and mild Sanfilippo B syndrome. No striking differences were demonstrated between the mutant enzymes from the severe and the mild case. However we found an altered enzyme activity characterized by displacement of the pH optimum towards basic values compared to the pH optimum of the normal enzyme, higher stability to heat and to Hg2+ ion treatment. It is suggested that the Sanfilippo B disease in this sibship is due to a mutation of a structural gene coding for alpha-N-acetylglucosaminidase.

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Year:  1982        PMID: 6809360     DOI: 10.1016/0009-8981(82)90273-x

Source DB:  PubMed          Journal:  Clin Chim Acta        ISSN: 0009-8981            Impact factor:   3.786


  3 in total

1.  Highly diverse phenotypes of mucopolysaccharidosis type IIIB sibling patients: effects of an additional mutation in the AUTS2 gene.

Authors:  Paulina Anikiej-Wiczenbach; Arkadiusz Mański; Katarzyna Milska-Musa; Monika Limanówka; Jolanta Wierzba; Aleksander Jamsheer; Zuzanna Cyske; Lidia Gaffke; Karolina Pierzynowska; Grzegorz Węgrzyn
Journal:  J Appl Genet       Date:  2022-05-08       Impact factor: 2.653

2.  Sanfilippo B disease: a re-examination of a particular sibship after 12 years.

Authors:  P Di Natale
Journal:  J Inherit Metab Dis       Date:  1991       Impact factor: 4.982

3.  Molecular defects in the alpha-N-acetylglucosaminidase gene in Italian Sanfilippo type B patients.

Authors:  A Tessitore; G R Villani; C Di Domenico; M Filocamo; R Gatti; P Di Natale
Journal:  Hum Genet       Date:  2000-12       Impact factor: 4.132

  3 in total

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