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Secondary mitochondrial dysfunction Multiple Acyl-CoA Dehydrogenase Deficiency (OMIM# 231680) Multiple acyl-coenzyme A dehydrogenase deficiency, also known as glutaric aciduria Type II (GAII), is an autosomal recessive disorder that affects the oxidation of fatty acids, BCAA, lysine, tryptophan, and choline
21, 2026 at 4:56 PM EDT | A Greenville physical therapist says patients who do prehab before surgery see up to a 40% improvement in outcomes
What shes told me of her personal situation is consistent with pernicious anemia even though she claims not to have pernicious anemia
Several other studies have not observed this association, suggesting the need for more knowledge in this area
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