Phospholipid and Glycolipid Metabolism Pt. II Flashcards
(38 cards)
Ganglioside Function

Biosynthesis of GM1

Glycosphingolipid Degredation

Which one of the following is another example of a lysosomal storage disease
Von Gierke Disease
Cori Disease
MCAD
Refsum
Pompe Disease
Pompe Disease — Build up of glycogen and loss of glucosidase activity in the lysosome.
Pathway I to Lactosyl Ceramide

Second Pathway to Lactosyl Ceramide

Lactosyl Ceramide to Ceramide

Second Pathway to Ceramide

Third Pathway to Ceramide

Common Features of the Sphingolipidoses

Generalized Gangliosidoses
Disease Name
Enzyme Efficiency
Elevated Lipid
Symptoms

Tay Sach’s Disease

Sandhoff’s Disease
Disease Name
Enzyme Efficiency
Elevated Lipid
Symptoms

Fabry’s Disease
Disease Name
Enzyme Efficiency
Elevated Lipid
Symptoms

Ceramide Lactoside Lipidosis
Disease Name
Enzyme Efficiency
Elevated Lipid
Symptoms

Metachromatic Leukodystrophy
Disease Name
Enzyme Efficiency
Elevated Lipid
Symptoms

Krabbe’s Disease
Disease Name
Enzyme Efficiency
Elevated Lipid
Symptoms

Guacher’s Disease
Disease Name
Enzyme Efficiency
Elevated Lipid
Symptoms

Niemann-Pick Disease
Disease Name
Enzyme Efficiency
Elevated Lipid
Symptoms

Farber’s Disease
Disease Name
Enzyme Efficiency
Elevated Lipid
Symptoms

What disease corresponds to the loss of Sailic Acid?
There is no disease is the loss of saillic acid.
Biochemical Basis for TaySach’s Disease

Biochemical Properties of Hexosaminidase A

Biochemical Properties of Hexosamindase B












