3-methylglutaconic aciduria type 3

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3-methylglutaconic aciduria type 3

Synonyms: Autosomal recessive optic atrophy plus syndrome | Autosomal recessive optic atrophy type 3 | Costeff optic atrophy syndrome | Costeff syndrome | Infantile optic atrophy with chorea and spastic paraplegia | MGA3

3-methylglutaconic aciduria type III (MGA III) is an organic aciduria characterised by the association of optic atrophy and choreoathetosis with 3-methylglutaconic aciduria.

Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.

Reference: Access aggregated data from Orphanet at Orphadata.

Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http: //www.orphadata.org. Data version September 2023.

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3-methylglutaconic aciduria type 3?

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Advocacy Organizations

Mississippi Metabolics Foundation

Mississippi Metabolics Foundation (MMF) was founded to raise awareness, educate, and provide support to those living or caring for someone with genetic metabolic disorders/inborn errors of metabolism (IEM).

Clinical Trials

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