Glycogen Storage Disease type III (Glycogenosis Type III)
Glycogen Storage Disease (GSD, Glycogenosis)

DEFINITION

Glycogen storage disease type III is an autosomal recessive metabolic disorder and inborn error of metabolism characterized by a deficiency in glycogen debranching enzymes.

Database	Link
The Diseases Database	GSD III
MedlinePlus	"GSD III":
OMIM single gene	GSD III
Wikigenes	AGL
GeneCards	AGL
Kegg Pathway	GSD III

EPIDEMIOLOGY

age, sex, seasonality, etc

SYMPTOMS

DIAGNOSIS

histopathology
radiology
NMR
laboratory tests

PATHOGENESIS

PATIENT RISK FACTORS

Vascular

Genetic

Acquired

Hormonal

Genetic

Acquired

TISSUE SPECIFIC RISK FACTORS

anatomical (due its structure)

vascular (due to the local circulation)

physiopathological (due to tissue function and activity)

COMPLICATIONS

THERAPY