Browse

Explore conditions, clinical trials, and the organisations running them.

Glycogen storage disease due to glycogen branching enzyme deficiency

Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases.

2 trials tagged with this condition →

Adult polyglucosan body disease 1 trial
Glycogen storage disease due to glycogen branching enzyme deficiency, adult neuromuscular form 0 trials
Glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form 0 trials
Glycogen storage disease due to glycogen branching enzyme deficiency, childhood neuromuscular form 0 trials
Glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form 0 trials
Glycogen storage disease due to glycogen branching enzyme deficiency, fatal perinatal neuromuscular form 0 trials
Glycogen storage disease due to glycogen branching enzyme deficiency, non progressive hepatic form 0 trials
Glycogen storage disease due to glycogen branching enzyme deficiency, progressive hepatic form 0 trials