Sphingolipidoses are a class of lipid storage disorders or degenerative storage disorders caused by deficiency of an enzyme that is required for the catabolism...

play important roles in signal transduction and cell recognition. Sphingolipidoses, or disorders of sphingolipid metabolism, have particular impact on...

Many lipid storage disorders can be classified into the subgroup of sphingolipidoses, as they relate to sphingolipid metabolism. Members of this group include...

(including Tay–Sachs disease (E75.0-E75.1) - they are a subtype of sphingolipidoses Sphingolipidoses that are not gangliosidoses, including Gaucher's and Niemann–Pick...

glycans from glycolipids to turn them back into unmodified lipids. Sphingolipidoses are a group of diseases that are associated with the accumulation of...

then solely formed via degradation of sphingolipid in the lysosome. Sphingolipidoses General structures of sphingolipids Dimethylsphingosine Fingolimod...

gangliosidoses such as Tay–Sachs disease. Ganglioside GM2 activator protein Sphingolipidoses Structures of GM1, GM2, GM3 gangliosides Guetta E, Peleg L (2008)....

commonly listed in the family of leukodystrophies as well as among the sphingolipidoses as it affects the metabolism of sphingolipids. Leukodystrophies affect...

Sphingolipidoses...

from necrosis and apoptosis occurring after acute spinal cord injury. Sphingolipidoses Structures of GM1, GM2, GM3 gangliosides Mocchetti I (2005). "Exogenous...

personality Anne Begg; Scottish politician Adam Rose; American actor Sphingolipidoses Lysosomal storage disease Niemann–Pick disease Fabry disease Tay–Sachs...

Niemann–Pick diseases are a subgroup of lipid storage disorders called sphingolipidoses in which harmful quantities of fatty substances, or lipids, accumulate...

Incorrect breakdown of these lipids leads to a group of diseases known as sphingolipidoses, which are often characterised by neurodegeneration and developmental...

pathology and ultrastructure and also different from other forms of sphingolipidoses.[citation needed] Subsequently, Santavuori and Haltia showed that an...

from the similarity in presentation to both mucopolysaccharidoses and sphingolipidoses. A biochemical understanding of these conditions has changed how they...

females equally. GM1 gangliosidoses - GM1 GM2 gangliosidoses - GM2 Sphingolipidoses#Overview Prayson, Richard A. (2012). Neuropathology. Elsevier Health...

shock protein-based therapy as a potential candidate for treating the sphingolipidoses". Science Translational Medicine. 8 (355): 355ra118. doi:10.1126/scitranslmed...

accumulation of GM1 gangliosides. They are inherited, autosomal recessive sphingolipidoses, a class of lipid storage disorders. Diagnosis of GM1 can be obtained...

for the Prevention of Recessive Genetic Disorders". Sphingolipids, Sphingolipidoses and Allied Disorders. Advances in Experimental Medicine and Biology...

Jansky–Bielschowsky disease (late infantile neuronal ceroid lipofuscinosis) Sphingolipidoses Niemann–Pick disease Gaucher disease Leukodystrophies Adrenoleukodystrophy...

glycogenosis type II, storage diseases (Gaucher, Niemann Pick and other sphingolipidoses) mitochondrial diseases and genetic immunodeficiencies such as IPEX...

and multiple sulfatase deficiency are classified as sulfatidoses. Sphingolipidoses#Overview for an overview table, including sulfatidosis "Definition:...

435.810 – sialic acid storage disease MeSH C18.452.100.100.435.825 – sphingolipidoses MeSH C18.452.100.100.435.825.200 – fabry disease MeSH C18.452.100.100...

435.810 – sialic acid storage disease MeSH C16.320.565.150.435.825 – sphingolipidoses MeSH C16.320.565.150.435.825.200 – Fabry disease MeSH C16.320.565.150...

810 – sialic acid storage disease MeSH C10.228.140.163.100.435.825 – sphingolipidoses MeSH C10.228.140.163.100.435.825.200 – fabry disease MeSH C10.228.140...