Ultrastructural study on a severe infantile sialidosis (beta-galactosidase-alpha-neuraminidase deficiency)

Neuropediatrics. 1985 May;16(2):109-12. doi: 10.1055/s-2008-1052553.

Abstract

This study was undertaken to elucidate ultrastructural changes in a severe infantile sialidosis. The materials examined in this study consisted of biopsied rectal mucosa and autopsied small intestine, liver and kidney. In the biopsy sample, axons contained a number of pleomorphic electron dense bodies, and numerous membrane-bound vacuoles were found in Schwann's cells, fibroblasts, endothelial cells, lymphocytes and plasma cells. In autopsy samples, neurons in Auerbach's myenteric plexus of the small intestine were filled with a number of membranous cytoplasmic bodies, pleomorphic dense bodies and vesicles containing dense materials. Hepatocytes in the liver, and glomerular and tubular epithelial cells in the kidney were also extended by a number of membrane-bound vacuoles. These ultrastructural changes in severe infantile sialidosis closely resemble those in GM1-gangliosidosis type 1.

Publication types

  • Case Reports
  • Comparative Study

MeSH terms

  • Biopsy
  • Female
  • Gangliosidoses / pathology
  • Humans
  • Infant
  • Intestinal Mucosa / ultrastructure*
  • Kidney / ultrastructure*
  • Lactose Intolerance / pathology*
  • Liver / ultrastructure*
  • Microscopy, Electron
  • Myenteric Plexus / ultrastructure
  • Neuraminidase / deficiency*

Substances

  • Neuraminidase