<abstract xmlns="http://www.w3.org/1999/xhtml"><sec id="j_1905-7415.1101.537_s_005_w2aab3b7b4b1b6b1aab1c17b1Aa"><h3>Background</h3><p>Classic organic acidurias, including isovaleric aciduria (IVA), propionic aciduria (PA) and methylmalonic aciduria (MMA), are rare inherited metabolic disorders caused by deficiencies of enzymes in catabolic pathways.</p></sec><sec id="j_1905-7415.1101.537_s_006_w2aab3b7b4b1b6b1aab1c17b2Aa"><h3>Objective</h3><p>To report clinical and laboratory findings and outcomes of classic organic acidurias in children north-eastern Thailand and their outcomes over the past 5 years.</p></sec><sec id="j_1905-7415.1101.537_s_007_w2aab3b7b4b1b6b1aab1c17b3Aa"><h3>Methods</h3><p>During 2010-2014, twelve patients were identified as having classic organic acidurias confirmed by urine organic acids analysis.</p></sec><sec id="j_1905-7415.1101.537_s_008_w2aab3b7b4b1b6b1aab1c17b4Aa"><h3>Results</h3><p>Classic organic acidurias were identified as follows; 5 patients with IVA, 4 patients with PA, and 3 patients with MMA. Ten patients had neonatal-onset and 9 cases were diagnosed during the neonatal period with clinical signs and symptoms of altered consciousness, poor feeding, respiratory distress, abnormal odor, and shock. Common laboratory findings included metabolic acidosis with an elevated anion gap, hyperammonemia, hypocalcemia, and cytopenia. Ammonia levels could be extremely high, especially in PA. Three patients with neonatal-onset of acidurias died during their first catabolic crisis, and one patient died later. One patient with MMA had exfoliative erythema after excessive dietary restriction. Four of 8 surviving patients had IVA and had better neurodevelopmental outcomes than those with PA and MMA.</p></sec><sec id="j_1905-7415.1101.537_s_009_w2aab3b7b4b1b6b1aab1c17b5Aa"><h3>Conclusions</h3><p>Neonatal-onset classic organic acidurias are more common than late-onset cases and usually mimic neonatal sepsis. Laboratory findings that include hematologic abnormalities should raise suspicion. Close monitoring of biochemical parameters, growth and neurodevelopmental outcomes is necessary in a long-term follow-up.</p></sec></abstract>

BackgroundClassic organic acidurias, including isovaleric aciduria (IVA), propionic aciduria (PA) and methylmalonic aciduria (MMA), are rare inherited metabolic disorders caused by deficiencies of enzymes in catabolic pathways.ObjectiveTo report clinical and laboratory findings and outcomes of classic organic acidurias in children north-eastern Thailand and their outcomes over the past 5 years.MethodsDuring 2010-2014, twelve patients were identified as having classic organic acidurias confirmed by urine organic acids analysis.ResultsClassic organic acidurias were identified as follows; 5 patients with IVA, 4 patients with PA, and 3 patients with MMA. Ten patients had neonatal-onset and 9 cases were diagnosed during the neonatal period with clinical signs and symptoms of altered consciousness, poor feeding, respiratory distress, abnormal odor, and shock. Common laboratory findings included metabolic acidosis with an elevated anion gap, hyperammonemia, hypocalcemia, and cytopenia. Ammonia levels could be extremely high, especially in PA. Three patients with neonatal-onset of acidurias died during their first catabolic crisis, and one patient died later. One patient with MMA had exfoliative erythema after excessive dietary restriction. Four of 8 surviving patients had IVA and had better neurodevelopmental outcomes than those with PA and MMA.ConclusionsNeonatal-onset classic organic acidurias are more common than late-onset cases and usually mimic neonatal sepsis. Laboratory findings that include hematologic abnormalities should raise suspicion. Close monitoring of biochemical parameters, growth and neurodevelopmental outcomes is necessary in a long-term follow-up.

Clinical and laboratory findings and outcomes of classic organic acidurias in children from north-eastern Thailand: a 5-year retrospective study

Department of Pediatrics, Faculty of Medicine

Asian Biomedicine

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

BackgroundClassic organic acidurias, including isovaleric aciduria (IVA), propionic aciduria (PA) and methylmalonic aciduria (MMA), are rare inherited...

Clinical and laboratory findings and outcomes of classic organic acidurias in children from north-eastern Thailand: a 5-year retrospective study

Article Category: Brief communication (Original)

Pubblicato online: 31 ago 2017

Pagine: 41 - 47

DOI: https://doi.org/10.5372/1905-7415.1101.537

Parole chiave
Isovaleric aciduria, methylmalonic aciduria, neutropenia, organic acidurias, propionic aciduria

© 2017 Khunton Wichajarn, Somporn Liammongkolkul, Nithiwat Vatanavicharn, Duangrurdee Wattanasirichaigoon

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

Clinical and laboratory findings and outcomes of classic organic acidurias in children from north-eastern Thailand: a 5-year retrospective study

Article Category: Brief communication (Original)

Pubblicato online: 31 ago 2017

Pagine: 41 - 47

DOI: https://doi.org/10.5372/1905-7415.1101.537

Parole chiaveIsovaleric aciduria, methylmalonic aciduria, neutropenia, organic acidurias, propionic aciduria

© 2017 Khunton Wichajarn, Somporn Liammongkolkul, Nithiwat Vatanavicharn, Duangrurdee Wattanasirichaigoon

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

Parole chiave
Isovaleric aciduria, methylmalonic aciduria, neutropenia, organic acidurias, propionic aciduria