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WorksheetsAll about GSDs
Total questions: 15
Worksheet time: 8mins
Which disease is autosomal recessive
Cori’s disease
Von Gierke’s disease
Anderson’s disease
Hers disease
Which GSD is characterised by infantile Cardiomegaly
Pompe’s disease
Coris disease
McArdles disease
Tarui’s disease
Which GSD mainly affects the skeletal muscle
Type I
Type II
Type VI
Type V
Which GSD is because of deficiency of Glucosyl 4-6 transferase (branching enzyme)
Anderson’s
Pompes
von Gierkes
Hers
Which GSD is responsible for severe fasting hypoglycaemia, lactic academia and hyperuricemia leading to gout
von Gierkes
Pompes
Anderson’s
Coris
Which GSD leads to increased accumulation of long insoluble glycogen chains
pompes
McArdles
Anderson’s
Coris
Which GSD is because of lysosomal Alfa 1-4 glucosidase
Hers
Pompes
Coris
Anderson’s
Which GSD is not because of extra glycogen storage in the liver
GSD 0
Type V
Type II
Type I
Hers disease is because of deficiency of which enzyme
Hepatic glycogen phosphorylase
Amylo Alfa 1,6 glucosidase
Phosphofructokinase
Muscle glycogen phosphorylase
Coris disease generally affects
Liver
Muscle
Heart and leukocytes
All
Which GSD is due to glucose 6 phosphatase deficiency
Type I
Type III
Type V
Type VI
Name of Type III GSD
Pompes
coris
McArdles
Hers
Which disease is characterised by diaphragm weakness leading to respiratory failure
Pompes
Coris
Von gierkes
Taruis
Anderson’s disease is because of deficiency of
Alfa 1,4 glucosidase
Alfa 1,6 glucosidase
Glucosyl 4,6 transferase
Glucose 6 phosphatase
Most common GSD
von Gierkes
Coris
Pompes
Anderson’s
