methylmalonic acid has been researched along with Erythrophagocytic Lymphohistiocytosis, Familial 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 |
---|---|---|
"Cobalamin C disease is a rare genetic condition resulting in methylmalonic aciduria, homocystinuria, and hematologic abnormalities." | 3.73 | Cobalamin C disease presenting with hemophagocytic lymphohistiocytosis. ( Coates, T; Gonzalez-Gomez, I; Wu, S; Yano, S, 2005) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Wu, S | 1 |
Gonzalez-Gomez, I | 1 |
Coates, T | 1 |
Yano, S | 1 |
1 other study available for methylmalonic acid and Erythrophagocytic Lymphohistiocytosis, Familial
Article | Year |
---|---|
Cobalamin C disease presenting with hemophagocytic lymphohistiocytosis.
Topics: Diagnosis, Differential; Female; Hemolytic-Uremic Syndrome; Homocystinuria; Humans; Infant; Lymphohi | 2005 |