Generalized accumulation of neutral glycosphingolipids with G M2 ganglioside accumulation in the brain.

Abstract

Analyses have been made of glycosphingolipids from visceral organs and brain of a patient with an unusual lipid storage disorder diagnosed initially as classical Tay-Sachs disease. Levels of the lipids from fresh-frozen sections of gray and white matter, kidney, spleen, liver, and heart from this patient were compared with those of normal juvenile controls, and the fatty acid composition of accumulated glycosphingolipids was compared with reference compounds. This patient was found to have abnormally high concentrations of a globoside in liver, kidney, and spleen, asialo G(M2) ganglioside in brain and liver, and G(M2) ganglioside in the brain. On the basis of these findings along with the clinical manifestations of Tay-Sachs disease with visceral involvement (hepatosplenomegaly) and demonstration of total deficiency of both A and B components of beta-N-acetylhexosaminidase activity, this glycosphingolipidosis is the same as two previously reported cases of G(M2) gangliosidosis with globoside accumulation and total beta-N-acetylhexosaminidase deficiency.

• Authors: P D Snyder Jr, W Krivit, C C Sweeley
• Journal: Journal of lipid research (J Lipid Res) Vol. 13 Issue 1 Pg. 128-36 (Jan 1972) ISSN: 0022-2275 [Print] United States
• PMID: 5059190 (Publication Type: Journal Article)

Chemical References

• Cerebrosides
• Fatty Acids
• Gangliosides
• Glycolipids
• Neuraminic Acids

Topics

• Brain (metabolism)
• Carbohydrate Metabolism, Inborn Errors (metabolism)
• Cerebrosides (analysis, metabolism)
• Chromatography, Gas
• Chromatography, Thin Layer
• Fatty Acids (analysis)
• Gangliosides (metabolism)
• Glycolipids (analysis, metabolism)
• Humans
• Infant
• Kidney (metabolism)
• Lipid Metabolism, Inborn Errors (metabolism)
• Lipidoses (metabolism)
• Liver (metabolism)
• Mass Spectrometry
• Neuraminic Acids (metabolism)
• Spleen (metabolism)