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Malonic aciduria

Also Known As:
Malonicaciduria; Malonyl-CoA decarboxylase deficiency; Malonyl-Coenzyme A Decarboxylase Deficiency
Networked: 25 relevant articles (1 outcomes, 1 trials/studies)

Relationship Network

Bio-Agent Context: Research Results

Experts

1. Salomons, Gajja S: 2 articles (11/2021 - 12/2014)
2. Abily-Donval, Lenaig: 1 article (11/2021)
3. Bekri, Soumeya: 1 article (11/2021)
4. Goldenberg, Alice: 1 article (11/2021)
5. Marret, Stéphane: 1 article (11/2021)
6. Snanoudj, Sarah: 1 article (11/2021)
7. Sudrié-Arnaud, Bénédicte: 1 article (11/2021)
8. Tebani, Abdellah: 1 article (11/2021)
9. Torre, Stéphanie: 1 article (11/2021)
10. Ko, Jung Min: 1 article (01/2020)

Related Diseases

1. Cardiomyopathies (Cardiomyopathy)
2. Seizures (Absence Seizure)
3. Propionic Acidemia
08/01/2017 - "Among these disorders, methyl malonic aciduria, propionic aciduria, maple syrup urine disease and isovaleric aciduria are sometimes referred to as classical organic acidurias. "
11/01/2023 - "The majority of tested candidate diseases were found to be suitable for inclusion in NBS programmes, while multiple acyl-CoA dehydrogenase deficiency, isolated methylmalonic acidurias, propionic acidemia and malonyl-CoA decarboxylase deficiency showed some and carnitine transporter defect significant limitations. "
04/01/2017 - "Five (5.7%) cases of MHBD (2-methyl-3-hydroxybutyryl-CoA), 4 (4.5%) each of PPA (propionic aciduria) and HMG-CoA lyase deficiency, 3 (3.4%) cases each of IVA (isovaleric aciduria), multiple carboxylase deficiency, fructose-1, 6-biphosphatase deficiency, fumarase deficiency, GA-1 (glutaric aciduria type 1) and 2 (2.3%) cases of EMA (ethyl-malonic aciduria). "
03/01/2015 - "Neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD) was the most common (153 cases), followed by methylmalonic aciduria (48 cases), urea cycle disorders (21 cases), phenylketonuria (20 cases), propionic aciduria (11 cases), X-linked adrenoleukodystrophy (10 cases), multiple carboxylase deficiency (8 cases), glutaric aciduria type I (7 cases), isovaleric aciduria (6 cases), glutaric aciduria type II (4 cases), short-chain acyl-CoA dehydrogenase deficiency (4 cases), 3-hydroxy-3-methylglutaric aciduria (3 cases), maple syrup urine disease (2 cases), very long-chain acyl-CoA dehydrogenase deficiency (1 case), malonic aciduria (1 case), mevalonic aciduria (1 case), Canavan disease (1 case), lysine protein intolerance (1 case), and medium-chain acyl-CoA dehydrogenase deficiency (1 case). "
4. Hypoglycemia (Reactive Hypoglycemia)
5. Acidosis

Related Drugs and Biologics

1. Methylmalonic Acid
2. malonic acid (malonate)
3. Enzymes
4. 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
5. Malonic aciduria
6. malonyl-CoA decarboxylase
7. Succinic Acid (Succinate)
8. Lactic Acid (Lactate)
9. Initiator Codon (Start Codon)
10. Valproic Acid (Depakote)

Related Therapies and Procedures

1. Secondary Prevention
2. Diet Therapy (Therapy, Diet)