Glycogen Storage Disease Type IV
"Glycogen Storage Disease Type IV" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
An autosomal recessive metabolic disorder due to a deficiency in expression of glycogen branching enzyme 1 (alpha-1,4-glucan-6-alpha-glucosyltransferase), resulting in an accumulation of abnormal GLYCOGEN with long outer branches. Clinical features are MUSCLE HYPOTONIA and CIRRHOSIS. Death from liver disease usually occurs before age 2.
|Glycogen Storage Disease Type IV
- Glycogen Storage Disease Type IV
- Andersen Disease
- Disease, Andersen
- Andersen's Disease
- Andersens Disease
- Disease, Andersen's
- Brancher Deficiency
- Brancher Deficiencies
- Deficiencies, Brancher
- Deficiency, Brancher
- Glycogen Branching Enzyme Deficiency
- Glycogen Storage Disease Type 4
- Glycogenosis 4
- Glycogenosis 4s
- Glycogenosis IV
- Glycogenosis IVs
- Type IV Glycogenosis
- Glycogenoses, Type IV
- Glycogenosis, Type IV
- Type IV Glycogenoses
- Gbe1 Deficiency
- Deficiencies, Gbe1
- Deficiency, Gbe1
- Gbe1 Deficiencies
Below are MeSH descriptors whose meaning is more general than "Glycogen Storage Disease Type IV".
Below are MeSH descriptors whose meaning is more specific than "Glycogen Storage Disease Type IV".
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Below are the most recent publications written about "Glycogen Storage Disease Type IV" by people in Profiles.
Anesthetic management in a child with Glycogen Storage Disease IV. Paediatr Anaesth. 2010 May; 20(5):475.