Korean J Pediatr.  2008 Sep;51(9):964-970. 10.3345/kjp.2008.51.9.964.

Genotype and clinical features of Korean patients with methylmalonic aciduria and propionic aciduria

• Lee EH
• Ko JM
• Kim JM
• Yoo HW

• KMID: 2280191
• DOI: http://doi.org/10.3345/kjp.2008.51.9.964

Abstract

PURPOSE
Methylmalonic aciduria (MMA) and propionic aciduria (PA) are inborn errors in the catabolism of branched-chain amino acids. The study was undertaken to investigate the genotypes and clinical features of Korean patients with MMA and PA. METHODS: This study examined 12 patients with MMA and eight with PA. We analyzed various clinical features, laboratory findings, treatments, and neuro-developmental outcomes. Diagnoses were based on the presence of characteristic compounds detected by amino acid analysis in serum and organic acid analysis in urine. Mutation analysis was performed in the genes of MUT, MMAA, MMAB, and MMACHC for MMA and PCCA and PCCB for PA. RESULTS: Among the 20 patients, six patients were diagnosed before one month of age and nine patients were diagnosed after the newborn period. Five patients were diagnosed via a neonatal screening test. Patients with early-onset forms had more severe illness at presentation and generally poor outcomes. A favorable outcome was obtained in 55% patients; most of them were of a late-onset type or diagnosed by neonatal mass screening test without symptoms. Genotypes were confirmed in all patients with MMA. We detected 11 different mutations by MUT gene analysis in 10 patients, and three different mutations in MMACHC genes in two patients. PCCA and PCCB gene mutations were identified in 14 of the 16 alleles, in eight patients with PA. CONCLUSION: Organic aciduria is a fatal disease; however, better outcomes are expected whenever early diagnosis and prompt management are made possible. Mutation analysis is useful for confirming diagnoses and planning management strategies.

Keyword

Methylmalonic aciduria; Propionic aciduria; MUT; MMACHC; PCCA; PCCB

MeSH Terms

Alleles
Amino Acids, Branched-Chain
Chromones
Diethylpropion
Early Diagnosis
Genotype
Humans
Infant, Newborn
Mass Screening
Neonatal Screening
Propionic Acidemia
Amino Acids, Branched-Chain
Chromones
Diethylpropion