Abstract
Four disorders of proline metabolism are known: two in its catabolism (hyperprolinaemia type I, which is due to proline oxidase deficiency, and hyperprolinaemia type II, which is due to ∆-pyrroline 5-carboxylate dehydrogenase deficiency) and two in its synthesis (∆1-pyrroline 5-carboxylate synthase deficiency and ∆-pyrroline 5-carboxylate reductase deficiency). Hyperprolinaemia type I is generally considered a nondisease, while hyperprolinaemia type II appears to be associated with a disposition to recurrent seizures. The deficiency of the proline-synthesising enzyme, ∆-pyrroline 5-carboxylate synthase, which is also involved in ornithine synthesis, is described in ► Chapter 22.
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Jaeken, J. (2012). Disorders of Proline and Serine Metabolism. In: Saudubray, JM., van den Berghe, G., Walter, J.H. (eds) Inborn Metabolic Diseases. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-15720-2_25
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DOI: https://doi.org/10.1007/978-3-642-15720-2_25
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