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J Inherit Metab Dis ; 25(1): 47-55, 2002 Feb.
Article in English | MEDLINE | ID: mdl-11999980

ABSTRACT

The lipid composition or the liver, spleen, brain, cerebellum and cerebrospinal fluid of a Gaucher disease type II patient who died at the age of 5 months was examined. The glycolipid analysis demonstrated a marked increase of total amounts not only in the peripheral tissues but also in the brain cerebellum and cerebrospinal fluid, with a prevalence of glucosylceramide. A reduction in gangliosides was observed in all the analysed tissues with a relative increase of GD3 in the nervous tissue. The fatty acid composition of glucosylceramide showed a prevalence of stearic acid in the central nervous system, while in the peripheral tissues palmitic acid was prevalent. This result suggests a different origin of the glucosylceramide stored in different tissues. The generalized reduction of gangliosides and their modified distribution together with the central nervous system GD3 increment represent a new observation. These data could be useful in the effort to clarify the pathophysiological mechanism of brain damage in neuronopathic Gaucher disease.


Subject(s)
Gaucher Disease , Glycolipids/analysis , Brain/pathology , Brain Chemistry , Cerebellum/chemistry , Cerebellum/pathology , Female , G(M1) Ganglioside/analysis , G(M1) Ganglioside/cerebrospinal fluid , Gangliosides/analysis , Gangliosides/cerebrospinal fluid , Gaucher Disease/cerebrospinal fluid , Gaucher Disease/pathology , Gaucher Disease/physiopathology , Glucosylceramides/analysis , Glucosylceramides/cerebrospinal fluid , Glycolipids/cerebrospinal fluid , Humans , Infant , Lactosylceramides/analysis , Lactosylceramides/cerebrospinal fluid , Liver/chemistry , Liver/pathology , Spleen/chemistry , Spleen/pathology
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