lactic acid has been researched along with Deaf Mutism in 6 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.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Maternally inherited diabetes and deafness (MIDD) and myoencephalopathy, lactic acidosis, stroke-like episodes (MELAS) syndromes are characterized by the same A3243G mutation of mitochondrial DNA (mtDNA)." | 3.75 | Brain anomalies in maternally inherited diabetes and deafness syndrome. ( Cozzone, PJ; Felician, O; Fromont, I; Lebail, B; Lefur, Y; Mancini, J; Nicoli, F; Paquis-Flucklinger, V; Valéro, R; Vialettes, B, 2009) |
| " This association is suggestive of the MIDD syndrome and the demonstration of metabolic abnormalities (raised serum lactic acid, abnormal lactate/pyruvate ratio) was compatible with a mitochondrial disease." | 3.74 | [Dilated cardiomyopathy, diabetes and deafness related to a mutation of mitochondrial DNA]. ( Charbonnier, B; Ferreira-Maldent, N; Guilmot, JL; Maillot, F; Quilliet, L, 2007) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (16.67) | 18.7374 |
| 1990's | 2 (33.33) | 18.2507 |
| 2000's | 2 (33.33) | 29.6817 |
| 2010's | 1 (16.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Fromont, I | 1 |
| Nicoli, F | 1 |
| Valéro, R | 1 |
| Felician, O | 1 |
| Lebail, B | 1 |
| Lefur, Y | 1 |
| Mancini, J | 1 |
| Paquis-Flucklinger, V | 1 |
| Cozzone, PJ | 1 |
| Vialettes, B | 1 |
| Machan, M | 1 |
| Kestenbaum, T | 1 |
| Fraga, GR | 1 |
| Ferreira-Maldent, N | 1 |
| Maillot, F | 1 |
| Quilliet, L | 1 |
| Guilmot, JL | 1 |
| Charbonnier, B | 1 |
| Bowen, J | 1 |
| Richards, T | 1 |
| Maravilla, K | 1 |
| Suzuki, S | 1 |
| Hinokio, Y | 1 |
| Ohtomo, M | 1 |
| Hirai, M | 1 |
| Hirai, A | 1 |
| Chiba, M | 1 |
| Kasuga, S | 1 |
| Satoh, Y | 1 |
| Akai, H | 1 |
| Toyota, T | 1 |
| Yoshida, Y | 1 |
| Katoh, Y | 1 |
| Shionoiri, H | 1 |
| Ishii, M | 1 |
1 trial available for lactic acid and Deaf Mutism
| Article | Year |
|---|---|
The effects of coenzyme Q10 treatment on maternally inherited diabetes mellitus and deafness, and mitochondrial DNA 3243 (A to G) mutation.
Topics: Adult; C-Peptide; Coenzymes; Deafness; Diabetes Complications; Diabetes Mellitus; Diabetic Nephropat | 1998 |
5 other studies available for lactic acid and Deaf Mutism
| Article | Year |
|---|---|
Brain anomalies in maternally inherited diabetes and deafness syndrome.
Topics: Adult; Aged; Brain; Cerebellar Ataxia; Cognition Disorders; Deafness; Diabetes Mellitus; Diabetes Me | 2009 |
Diffuse hyperkeratosis in a deaf and blind 48-year-old woman--quiz case. Diagnosis: keratitis-ichthyosis-deafness (KID) syndrome with secondary dermatophytosis.
Topics: Antifungal Agents; Baths; Blindness; Deafness; Dermatologic Agents; Female; Fluconazole; Humans; Ich | 2012 |
[Dilated cardiomyopathy, diabetes and deafness related to a mutation of mitochondrial DNA].
Topics: Cardiomyopathy, Dilated; Deafness; Diabetes Mellitus; DNA, Mitochondrial; Female; Humans; Lactic Aci | 2007 |
MR imaging and proton MR spectroscopy in A-to-G substitution at nucleotide position 3243 of leucine transfer RNA.
Topics: Adult; Amino Acid Substitution; Aspartic Acid; Basal Ganglia; Base Sequence; Brain; Cerebral Cortex; | 1998 |
[A case of idiopathic hypoparathyroidism associated with perceptive deafness and psoriasis vulgaris].
Topics: Adult; Calcium Metabolism Disorders; Deafness; Humans; Hypoparathyroidism; Lactates; Lactic Acid; Ma | 1988 |