type 4 glycogenosis

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type 4 glycogenosis

Glycogenosis due to brancher enzyme deficiency, resulting in the accumulation of abnormal glycogen in liver, kidney, muscle, and other tissues and characterized by progressive cirrhosis of the liver, leading to liver failure and death, usually before age 2. Also called Andersen's disease, brancher deficiency amylopectinosis.

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Andersen's disease
brancher deficiency amylopectinosis
Cori's disease
debrancher deficiency limit dextrinosis

Forbes disease
generalized glycogenosis
Gierke's disease
Hers disease

McArdle's disease
McArdle-Schmid-Pearson disease
Pompe's disease
type 1 glycogenosis

type 2 glycogenosis
type 3 glycogenosis
type 5 glycogenosis
type 6 glycogenosis

von Gierke's disease

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