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Glutaric aciduria type 1 (medical condition): A rare inherited metabolic disorder where a genetic mutation results in the deficiency of an enzyme called glutaryl-CoA dehydrogenase which is required to metabolise certain amino acids (lysine, hydroxylysine and tryptophan). Problems occur when these metabolites build up in the body and cause neurological problems. Symptoms often develop following an acute infection or fasting. The severity of the condition is highly variable from development of neurological symptoms during infancy to asymptomatic adults. The degree of enzyme deficiency will usually determine the severity.
See also:
Glutaricaciduria type 1:
»Introduction: Glutaricaciduria type 1
»Symptoms of Glutaricaciduria type 1
»Causes of Glutaricaciduria type 1
»Treatments for Glutaricaciduria type 1
These medical condition or symptom topics may be relevant to medical information for Glutaric aciduria type 1:
Ophanet, a consortium of European partners,
currently defines a condition rare when if affects 1 person per 2,000.
They list Glutaric aciduria type 1 as a "rare disease".
Source - Orphanet
Glutaric aciduria type 1 (medical condition): See Glutaricaciduria type 1 (disease information).
»Introduction: Glutaricaciduria type 1
»Symptoms of Glutaricaciduria type 1
»Causes of Glutaricaciduria type 1
»Treatments for Glutaricaciduria type 1
Source: Diseases Database
Source: Diseases Database
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