Disorders of Glycosphingolipid Metabolism
GM1 Gangliosidoses
Generalized GM1 Type II - Juvenile Form
Generalized GM1 Type III - Adult Form
The GM2 Gangliosidoses
Tay-Sachs Disease
GM2 Activator Deficiency
Sandhoff Disease
GM3 Gangliosidosis
Gaucher Disease
Niemann-Pick Disease, Type A and B
Types A and B are due to acid sphingomyelinase deficienciesNiemann-Pick Disease, Type C1
Niemann-Pick Disease, Type C2
Niemann-Pick Disease, Type D
Types C and D are not due to acid sphingomyelinase deficienciesSchindler Disease
Fabry Disease
Lactosylceramidosis
Farber Disease
Krabbe Disease
Multiple Sulfatase Deficiency - Austin Disease
Metachromic Leukodystrophy - Sulfatide Lipodosis
Fucosidosis
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Michael W. King, Ph.D / IU School of Medicine / miking at iupui.edu