| Literature DB >> 6775621 |
M G Hadfield, N R Ghatak, I Nakoneczna, H R Lippman, E C Myer, G Constantopoulos, R M Bradley.
Abstract
The pathologic changes in a rare case of mucopolysaccharidosis (MPS) type IIIB or Sanfilippo's syndrome B (absence of alpha-N-acetylglucosaminidase) are presented, along with the biochemical findings. Comparisons were made with other reported cases of MPS III subtypes and related storage disorders in terms of clinical, light microscopic, electron microscopic, and chemical findings, and a correlation of the ultrastructural changes made with the severe neurological dysfunction noted in this disorder. At present, MPS III subtypes cannot be separated from one another by morphological means because the same expression and distribution of lesions may be encountered among differing subtypes.Entities:
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Year: 1980 PMID: 6775621 DOI: 10.1001/archneur.1980.00500590069012
Source DB: PubMed Journal: Arch Neurol ISSN: 0003-9942