Glutaric aciduria type 2 (medical condition): A metabolic disorder involving an enzyme deficiency - electron transfer flavoprotein ubiquinone oxydoreductase. The severity of symptoms depends on the level of deficiency. The infant onset form is the most severe.
See also:
Electron Transfer Flavoprotein, deficiency of:
»Introduction: Electron Transfer Flavoprotein, deficiency of
»Symptoms of Electron Transfer Flavoprotein, deficiency of
These medical condition or symptom topics may be relevant to medical information for Glutaric aciduria type 2:
Ophanet, a consortium of European partners,
currently defines a condition rare when if affects 1 person per 2,000.
They list Glutaric aciduria type 2 as a "rare disease".
Source - Orphanet
Glutaric aciduria type 2: Another name for Electron Transfer Flavoprotein, deficiency of (or close medical condition association).
»Introduction: Electron Transfer Flavoprotein, deficiency of
»Symptoms of Electron Transfer Flavoprotein, deficiency of
Some of the symptoms of Glutaric aciduria type 2 incude:
Source: Diseases Database
Source: Diseases Database
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