Title : Ultrastructural study on a severe infantile sialidosis (beta-galactosidase-alpha-neuraminidase deficiency) - Yamano_1985_Neuropediatrics_16_109 |
Author(s) : Yamano T , Shimada M , Sugino H , Dezawa T , Koike M , Okada S , Yabuuchi H |
Ref : Neuropediatrics , 16 :109 , 1985 |
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. |
PubMedSearch : Yamano_1985_Neuropediatrics_16_109 |
PubMedID: 3925363 |
Gene_locus related to this paper: human-CTSA |
Gene_locus | human-CTSA |
Disease | Galactosialidosis |
Yamano T, Shimada M, Sugino H, Dezawa T, Koike M, Okada S, Yabuuchi H (1985)
Ultrastructural study on a severe infantile sialidosis (beta-galactosidase-alpha-neuraminidase deficiency)
Neuropediatrics
16 :109
Yamano T, Shimada M, Sugino H, Dezawa T, Koike M, Okada S, Yabuuchi H (1985)
Neuropediatrics
16 :109