About The Medical Condition Glycogen Storage Disease Type III
Find the definition of the medical term Glycogen Storage Disease Type III. Glycogen Storage Disease Type III defined and explained for easy understanding at the Medical Conditions from ClusterMed.info.
Glycogen Storage Disease Type III
| Glycogen Storage Disease Type III Medical Condition |
|---|
What's The Definition Of The Medical Condition Glycogen Storage Disease Type III?
An autosomal recessive metabolic disorder due to deficient expression of amylo-1,6-glucosidase (one part of the glycogen debranching enzyme system). The clinical course of the disease is similar to that of glycogen storage disease type I, but milder. Massive hepatomegaly, which is present in young children, diminishes and occasionally disappears with age. Levels of glycogen with short outer branches are elevated in muscle, liver, and erythrocytes. Six subgroups have been identified, with subgroups Type IIIa and Type IIIb being the most prevalent.
|
More Medical Conditions
A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | Q | R | S | T | U | V | W | X | Y | Z
Medical Conditions Definitions Of The Day
- Trophoblastic Neoplasms ‐ Trophoblastic growth, which may be gestational or nongestational…
- Acetohydroxy Acid Reductoisomerase ‐ An enzyme involved in the biosynthesis of isoleucine and valine.…
- Misoprostol, (11alpha,13E,16R)-Isomer ‐ A synthetic analog of natural prostaglandin E1. It produces a…
- Phobia ‐ Anxiety disorders in which the essential feature is persistent…
- Proton-Translocating ATPases, Bacterial ‐ Membrane-bound proton-translocating ATPases that serve two important…
- Apoenzymes ‐ The protein components of the enzyme minus any cofactors or prosthetic…
- Neck Dissections, Radical ‐ The most commonly performed major operation for head and neck…
- Activations, Amino Acid ‐ The first step of protein synthesis, whereby an amino acid reacts…
- Acupoints ‐ Designated locations along nerves or organ meridians for inserting…
- Deficiency Disease, Apolipoprotein B ‐ A disorder of lipid metabolism inherited as an autosomal recessive…