Similar Diseases
- Amylopectinosis
- Amylo 1,6 glucosidase deficiency
- Glycogen storage disease IX
- Glycogenosis type 9A
- Glycogenosis due to liver glycogen phosphorylase deficiency
- Glycogenosis due to muscle glycogen phosphorylase deficiency
- Glycogenin Deficiency
- Glycogenosis due to liver and muscle phosphorylase kinase deficiency
- Acid maltase deficiency
- Glycogenosis due to muscle phosphorylase kinase deficiency
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Results for Query ‹ Amylopectinosis risk ›
Glycogen storage disease type IV – In animals
In horses: it has been reported in American Quarter Horses and related breeds.
In cats: the disease has been reported in the Norwegian Forest Cat, where it causes skeletal muscle, heart, and CNS degeneration in animals greater than 5 months old. It has not been associated with cirrhosis or liver failure.
Glycogen storage disease type IV – Names
It is also known as:
- Glycogenosis type IV
- Glycogen branching enzyme deficiency
- Polyglucosan body disease
- Amylopectinosis
The eponym "Andersen's disease" is sometimes used, for Dorothy Hansine Andersen.
Mutations in GBE1 can also cause a milder disease in adults called adult polyglucosan body disease.