lactic acid has been researched along with Optic Atrophy, Hereditary, Leber in 1 studies
Lactic Acid: A normal intermediate in the fermentation (oxidation, metabolism) of sugar. The concentrated form is used internally to prevent gastrointestinal fermentation. (From Stedman, 26th ed)
2-hydroxypropanoic acid : A 2-hydroxy monocarboxylic acid that is propanoic acid in which one of the alpha-hydrogens is replaced by a hydroxy group.
Optic Atrophy, Hereditary, Leber: A maternally linked genetic disorder that presents in mid-life as acute or subacute central vision loss leading to central scotoma and blindness. The disease has been associated with missense mutations in the mtDNA, in genes for Complex I, III, and IV polypeptides, that can act autonomously or in association with each other to cause the disease. (from Online Mendelian Inheritance in Man, http://www.ncbi.nlm.nih.gov/Omim/, MIM#535000 (April 17, 2001))
| 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 |
|---|---|
| Gropman, A | 1 |
| Chen, TJ | 1 |
| Perng, CL | 1 |
| Krasnewich, D | 1 |
| Chernoff, E | 1 |
| Tifft, C | 1 |
| Wong, LJ | 1 |
1 other study available for lactic acid and Optic Atrophy, Hereditary, Leber
| Article | Year |
|---|---|
Variable clinical manifestation of homoplasmic G14459A mitochondrial DNA mutation.
Topics: Adult; Age of Onset; Child; Child, Preschool; DNA, Mitochondrial; Dystonia; Female; Humans; Lactic A | 2004 |