MGA 4: Introduction
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.
More detailed information about the symptoms,
causes, and treatments of MGA 4 is available below.
Symptoms of MGA 4
See full list of 14
symptoms of MGA 4
Home Diagnostic Testing
Home medical testing related to MGA 4:
- Bladder & Urinary Health: Home Testing:
Wrongly Diagnosed with MGA 4?
Causes of MGA 4
Read more about causes of MGA 4.
MGA 4: Undiagnosed Conditions
Commonly undiagnosed diseases in related medical categories:
Misdiagnosis and MGA 4
Interstitial cystitis an under-diagnosed bladder condition: The medical
condition of interstitial cystitic is a bladder condition that can be
misdiagnosed as...read more »
Read more about Misdiagnosis and MGA 4
MGA 4: Research Doctors & Specialists
Research related physicians and medical specialists:
- Urinary & Bladder Specialists (Urology):
- Kidney Health Specialists (Nephrology):
- more specialists...»
Other doctor, physician and specialist research services:
Statistics for MGA 4
MGA 4: Broader Related Topics
Types of MGA 4
User Interactive Forums
Read about other experiences, ask a question about MGA 4, or answer someone else's question, on our message boards:
Definitions of MGA 4:
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
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