Answers are grounded in this paper and cite their sources.
A patient with protein-losing gastroenteropathy and egg allergy has been shown to have a previously unrecognized organic aciduria, D-2-hydroxyglutaric aciduria. The observations made are consistent with an inherited metabolic disorder in the catabolism of 5-aminolaevulinate possibly due to deficient activity of a specific D-2-hydroxyglutarate dehydrogenase.
No takes yet. Share an insight, caveat, or question.
Chalmers et al. (1980) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: