Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Disorder of methylamine metabolism
Dimethylglycine dehydrogenase deficiency
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. This is an n-of-1 use case where only one patient or family has been described with this disorder.
-
Trimethylaminuria 2 trials Sub-types →