Dietary therapy in two patients with vitamin B12-unresponsive methylmalonic acidemia
- 1 February 1981
- journal article
- research article
- Published by Springer Nature in European Journal of Pediatrics
- Vol. 135 (3) , 305-312
- https://doi.org/10.1007/bf00442109
Abstract
The biochemical and therapeutic responses to dietary therapy were studied in a 25-month-old girl and a 1-month-old girl with methylmalonic acidemia (MMA-emia), which was unresponsive to vitamin B12. The minimum daily intake of protein which patients could tolerate and display a good development was between 1.0 and 1.2 g per kg body weight. Supplementation with amino acid mixture devoid of toxic amino acids was required to prevent protein malnutrition when daily protein intake was restricted to 0.6 g per kg body weight. Caloric intake should be sufficient, not only to promote growth but also to prevent a rise in MMA level, especially when a patient has ketoacidosis. It was found that MMA excretion per mg creatinine in random urine specimens correlated significantly with serum MMA and twenty four-hour output of MMA per kg body weight. Therefore measurement of MMA in a single urine specimen is useful for evaluating the in vivo accumulation of MMA.Keywords
This publication has 17 references indexed in Scilit:
- Methylmalonyl-CoA mutase deficiency associated with severe neonatal hyperammonemia: Activity of urea cycle enzymesThe Journal of Pediatrics, 1978
- Plasma Free Amino Acids in Normal Children and in Patients with Proteinocaloric Malnutrition: Fasting and InfectionPediatric Research, 1978
- Severe hyperammonemia in a newborn infant with methylmalonyl-CoA mutase deficiencyThe Journal of Pediatrics, 1978
- Methylmalonic aciduria: A variant form of methylmalonyl coenzyme A apomutase deficiencyThe Journal of Pediatrics, 1977
- Methylmalonyl-CoA mutase activity of leukocytes in variants and heterozygotes of methylmalonic acidemia.The Tohoku Journal of Experimental Medicine, 1977
- Microdetermination of methylmalonic acid and other short chain dicarboxylic acids by gas chromatography: Use in prenatal diagnosis of methylmalonic acidemia and in studies of isovaleric acidemiaClinica Chimica Acta; International Journal of Clinical Chemistry, 1976
- A simplified and rapid quantitative assay for propionic and methylmalonic acids in urine.1975
- Observations on the coexistence of methylmalonic acidemia and glycinemiaThe Journal of Pediatrics, 1969
- METHYLMALONIC ACIDEMIA A Disorder Associated with Acidosis, Hyperglycinemia, and HyperlactatemiaActa Paediatrica, 1968
- Methylmalonic aciduria. An inborn error of metabolism leading to chronic metabolic acidosis.Archives of Disease in Childhood, 1967