methylmalonic acid has been researched along with MODS in 1 studies
Methylmalonic Acid: A malonic acid derivative which is a vital intermediate in the metabolism of fat and protein. Abnormalities in methylmalonic acid metabolism lead to methylmalonic aciduria. This metabolic disease is attributed to a block in the enzymatic conversion of methylmalonyl CoA to succinyl CoA.
methylmalonic acid : A dicarboxylic acid that is malonic acid in which one of the methylene hydrogens is substituted by a methyl group.
Excerpt | Relevance | Reference |
---|---|---|
"The aim of this study was to identify the causative genetic lesion in two apparently unrelated newborns having lethal lactic acidosis, multi-organ failure and congenital malformations including interrupted aortic arch, who exhibited mild methylmalonic aciduria, combined mitochondrial respiratory chain deficiency, and marked muscle mitochondrial DNA depletion." | 3.76 | Marked mitochondrial DNA depletion associated with a novel SUCLG1 gene mutation resulting in lethal neonatal acidosis, multi-organ failure, and interrupted aortic arch. ( Andreu, AL; Arenas, J; Arroyo, I; Bornstein, B; Gallardo, E; Garesse, R; Marti, R; Martin, MA; Martinez-Pardo, M; Merinero, B; Moran, MJ; Perez-Jurado, LA; Rivera, H; Ruiz-Sala, P; Serra-Suhe, C; Ugalde, C; Ugarte, M, 2010) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (100.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Rivera, H | 1 |
Merinero, B | 1 |
Martinez-Pardo, M | 1 |
Arroyo, I | 1 |
Ruiz-Sala, P | 1 |
Bornstein, B | 1 |
Serra-Suhe, C | 1 |
Gallardo, E | 1 |
Marti, R | 1 |
Moran, MJ | 1 |
Ugalde, C | 1 |
Perez-Jurado, LA | 1 |
Andreu, AL | 1 |
Garesse, R | 1 |
Ugarte, M | 1 |
Arenas, J | 1 |
Martin, MA | 1 |
1 other study available for methylmalonic acid and MODS
Article | Year |
---|---|
Marked mitochondrial DNA depletion associated with a novel SUCLG1 gene mutation resulting in lethal neonatal acidosis, multi-organ failure, and interrupted aortic arch.
Topics: Acidosis; Aorta, Thoracic; DNA, Mitochondrial; Fatal Outcome; Female; Genetic Diseases, Inborn; Huma | 2010 |