Dimethylglycine dehydrogenase deficiency

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Synonyms: DMG dehydrogenase deficiency | DMGDH deficiency

Dimethylglycine dehydrogenase deficiency is an extremely rare autosomal recessive glycine metabolism disorder characterized clinically in the single reported case to date by muscle fatigue and a fish-like odor.

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 June 2024

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Dimethylglycine dehydrogenase deficiency?

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Clinical Trials

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