Glycogen storage disease due to glycogen branching enzyme deficiency
MONDO:0009292Glycogen 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.
Also known as: Andersen Disease (GSD IV), Andersen disease, Andersen's disease, GBE1 glycogen storage disease, GSD due to glycogen branching enzyme deficiency, GSD type 4, GSD type IV, amylopectinosis
2 clinical trials for this condition and its sub-types, 2 tagged with Glycogen storage disease due to glycogen branching enzyme deficiency itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Glycogen storage disease due to glycogen branching enzyme deficiency
-
Adult polyglucosan body disease 1 trial
-
Can a national registry unlock the genetic secrets of glycogen storage diseases in indian children?
Knowledge-focused Recruiting nowThis study aims to create a nationwide registry of Indian children with hepatic glycogen storage diseases (GSDs), a group of inherited metabolic disorders affecting the liver and muscles. By collecting genetic, clinical, and outcome data from 250 children, researchers hope to map…
Sponsor: Institute of Liver and Biliary Sciences, India • Aim: Knowledge-focused
Last updated Aug 07, 2026 00:00 UTC
-
Researchers track rare disease progression in GSD IV and APBD patients
Knowledge-focused Recruiting nowThis study gathers medical information from 200 people with glycogen branching enzyme deficiency, known as GSD IV or APBD. The goal is to learn how these rare diseases progress over time. No new treatments are tested; instead, researchers review clinic records to better understan…
Sponsor: Duke University • Aim: Knowledge-focused
Last updated Jun 27, 2026 12:29 UTC