Last update 23 Jan 2025

2-Methylbutyryl-CoA Dehydrogenase Deficiency

Basic Info

Synonyms
2-@METHYLBUTYRYL-CoA DEHYDROGENASE DEFICIENCY, 2-MBCD Deficiency, 2-METHYLBUTYRYL GLYCINURIA
+ [17]
Introduction
A rare organic aciduria characterized by impaired isoleucine degradation with increased plasma or whole blood C5 acylcarnitine levels (typically observed in newborn screening) and increased urinary excretion of N-methylbutyrylglycine. The condition is usually clinically asymptomatic, although patients with muscular hypotonia, developmental delay, and seizures (among others) have been reported.

Analysis

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