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Diseases » MGA 4 » Summary
 

What is MGA 4?

What is MGA 4?

  • MGA 4: MGA (methylglutaconic aciduria) is a rare genetic disorder where the body's cells are unable to make sufficient energy resulting in an accumulation in the body of 3-methylglutaconic acid. Type 4 is characterized by symptoms which overlap type 1 and 3.

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list MGA 4 as a "rare disease".
Source - Orphanet

MGA 4: Introduction

Types of MGA 4:

Broader types of MGA 4:

What causes MGA 4?

Causes of MGA 4: see causes of MGA 4
Cause of MGA 4: The condition is inherited in an autosomal recessive manner.

What are the symptoms of MGA 4?

Symptoms of MGA 4: see symptoms of MGA 4

MGA 4: Testing

Diagnostic testing: see tests for MGA 4.

Misdiagnosis: see misdiagnosis and MGA 4.

How is it treated?

Treatments for MGA 4: see treatments for MGA 4

Name of MGA 4

Main name of condition: MGA 4

 

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