Branched-chain organic acidurias/acidaemias

Helene Ogier De Baulny, Carlo Dionisi-Vici, Udo Wendel

Research output: Chapter in Book/Report/Conference proceedingChapter

22 Citations (Scopus)

Abstract

Branched-chain organic acidurias or organic acidaemias are a group of disorders that result from an abnormality of specific enzymes involving the catabolism of branched-chain amino acids (BCAAs). Collectively, the most commonly encountered are maple syrup urine disease (MSUD), isovaleric aciduria (IVA), propionic aciduria (PA) and methyl malonic aciduria (MMA). They can present clinically as a severe neonatal-onset form of metabolic distress, an acute and intermittent late-onset form, or a chronic progressive form presenting as hypotonia, failure to thrive, and developmental delay. Other rare disorders involving leucine, isoleucine, and valine catabolism are 3-methylcrotonyl glycinuria, 3-methylglutaconic (3-MGC) aciduria, short-/branched-chain acyl-CoA dehydrogenase deficiency, 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency, isobutyryl-CoA dehydrogenase deficiency, 3-hydroxyisobutyric aciduria, and malonic aciduria.

Original languageEnglish
Title of host publicationInborn Metabolic Diseases: Diagnosis and Treatment
PublisherSpringer Berlin Heidelberg
Pages277-296
Number of pages20
ISBN (Print)9783642157202, 9783642157196
DOIs
Publication statusPublished - Jan 1 2012

Fingerprint

Propionic Acidemia
Maple Syrup Urine Disease
Failure to Thrive
Branched Chain Amino Acids
Muscle Hypotonia
Isoleucine
Valine
Leucine
Enzymes
Malonic aciduria
2-Methylbutyryl-CoA Dehydrogenase Deficiency
3-Methylglutaconic Aciduria
Isobutyryl-CoA dehydrogenase deficiency
3-Hydroxyisobutyric aciduria
Hydroxyacyl-CoA Dehydrogenase, Type 2, Deficiency

ASJC Scopus subject areas

  • Medicine(all)

Cite this

De Baulny, H. O., Dionisi-Vici, C., & Wendel, U. (2012). Branched-chain organic acidurias/acidaemias. In Inborn Metabolic Diseases: Diagnosis and Treatment (pp. 277-296). Springer Berlin Heidelberg. https://doi.org/10.1007/978-3-642-15720-2_19

Branched-chain organic acidurias/acidaemias. / De Baulny, Helene Ogier; Dionisi-Vici, Carlo; Wendel, Udo.

Inborn Metabolic Diseases: Diagnosis and Treatment. Springer Berlin Heidelberg, 2012. p. 277-296.

Research output: Chapter in Book/Report/Conference proceedingChapter

De Baulny, HO, Dionisi-Vici, C & Wendel, U 2012, Branched-chain organic acidurias/acidaemias. in Inborn Metabolic Diseases: Diagnosis and Treatment. Springer Berlin Heidelberg, pp. 277-296. https://doi.org/10.1007/978-3-642-15720-2_19
De Baulny HO, Dionisi-Vici C, Wendel U. Branched-chain organic acidurias/acidaemias. In Inborn Metabolic Diseases: Diagnosis and Treatment. Springer Berlin Heidelberg. 2012. p. 277-296 https://doi.org/10.1007/978-3-642-15720-2_19
De Baulny, Helene Ogier ; Dionisi-Vici, Carlo ; Wendel, Udo. / Branched-chain organic acidurias/acidaemias. Inborn Metabolic Diseases: Diagnosis and Treatment. Springer Berlin Heidelberg, 2012. pp. 277-296
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