lactic acid has been researched along with Dystonia in 5 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.
Dystonia: An attitude or posture due to the co-contraction of agonists and antagonist muscles in one region of the body. It most often affects the large axial muscles of the trunk and limb girdles. Conditions which feature persistent or recurrent episodes of dystonia as a primary manifestation of disease are referred to as DYSTONIC DISORDERS. (Adams et al., Principles of Neurology, 6th ed, p77)
| Excerpt | Relevance | Reference |
|---|---|---|
| "Mitochondrial disorders are clinically heterogeneous." | 1.35 | Mitochondrial diseases mimicking neurotransmitter defects. ( Artuch, R; Briones, P; Carrilho, I; Duarte, S; Garcia-Cazorla, A; Garesse, R; Montoya, J; Nascimento, A; Ormazabal, A; Pineda, M; Sala-Castellvi, P; Serrano, M, 2008) |
| "Both patients had PDH deficiency caused by a new mutation (G585C) in the PDHA1 gene, which is predicted to replace a highly conserved glycine at codon 195 by alanine." | 1.35 | Pyruvate dehydrogenase deficiency presenting as intermittent isolated acute ataxia. ( Debray, FG; Gagne, R; Laframboise, R; Lambert, M; MacKay, N; Maranda, B; Mitchell, GA; Robinson, BH, 2008) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 4 (80.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (20.00) | 2.80 |
| Authors | Studies |
|---|---|
| de Gusmao, CM | 1 |
| Peixoto de Barcelos, I | 1 |
| Pinto, ALR | 1 |
| Silveira-Moriyama, L | 1 |
| Garcia-Cazorla, A | 1 |
| Duarte, S | 1 |
| Serrano, M | 1 |
| Nascimento, A | 1 |
| Ormazabal, A | 1 |
| Carrilho, I | 1 |
| Briones, P | 1 |
| Montoya, J | 1 |
| Garesse, R | 1 |
| Sala-Castellvi, P | 1 |
| Pineda, M | 1 |
| Artuch, R | 1 |
| Gropman, A | 1 |
| Chen, TJ | 1 |
| Perng, CL | 1 |
| Krasnewich, D | 1 |
| Chernoff, E | 1 |
| Tifft, C | 1 |
| Wong, LJ | 1 |
| Karagulle Kendi, AT | 1 |
| Krenzel, C | 1 |
| Ott, FW | 1 |
| Brace, JR | 1 |
| Norberg, SK | 1 |
| Kieffer, SA | 1 |
| Debray, FG | 1 |
| Lambert, M | 1 |
| Gagne, R | 1 |
| Maranda, B | 1 |
| Laframboise, R | 1 |
| MacKay, N | 1 |
| Robinson, BH | 1 |
| Mitchell, GA | 1 |
5 other studies available for lactic acid and Dystonia
| Article | Year |
|---|---|
Pearls & Oy-sters: Paroxysmal Exercise-Induced Dyskinesias Due to Pyruvate Dehydrogenase Deficiency.
Topics: Child, Preschool; Chorea; Dystonia; Humans; Lactic Acid; Male; Pyruvate Dehydrogenase Complex Defici | 2023 |
Mitochondrial diseases mimicking neurotransmitter defects.
Topics: Alanine; Brain; Child, Preschool; Consanguinity; Diagnosis, Differential; Dopamine Agents; Dystonia; | 2008 |
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 |
Poststreptococcal dystonia with bilateral striatal enlargement: MR imaging and spectroscopic findings.
Topics: Aspartic Acid; Autoantibodies; Bacterial Proteins; Caudate Nucleus; Child; Deoxyribonucleases; Diffu | 2008 |
Pyruvate dehydrogenase deficiency presenting as intermittent isolated acute ataxia.
Topics: Ataxia; Basal Ganglia Diseases; Binding Sites; Brain Diseases, Metabolic; Child; Child, Preschool; D | 2008 |