lactic acid has been researched along with Benign Infantile Myoclonic Epilepsy in 7 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 |
|---|---|---|
| "A case of a unique combination of mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like syndrome (MELAS) with acanthocytosis is reported." | 7.67 | Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes with acanthocytosis: a clinicopathological study of a unique case. ( Kazui, H; Mukoyama, M; Nonaka, I; Satoyoshi, E; Sunohara, N; Yoshida, M, 1986) |
| "A case of a unique combination of mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like syndrome (MELAS) with acanthocytosis is reported." | 3.67 | Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes with acanthocytosis: a clinicopathological study of a unique case. ( Kazui, H; Mukoyama, M; Nonaka, I; Satoyoshi, E; Sunohara, N; Yoshida, M, 1986) |
| "The disorders causing myoclonus have been compared to those in which myoclonus has been reported." | 2.37 | Myoclonus and mitochondrial myopathy. ( Hopkins, LC; Rosing, HS, 1986) |
| "At 3 years old, astatic myoclonic epilepsy appeared, with no response to levetiracetam." | 1.43 | Lysine Restriction and Pyridoxal Phosphate Administration in a NADK2 Patient. ( García-Villoria, J; Girós, M; Ribes, A; Ruiz, A; Torres, MA; Tort, F; Ugarteburu, O, 2016) |
| "Characteristics of myoclonic epilepsy associated with ragged-red fibers include myoclonic epilepsy, generalized epilepsy, hearing loss, exercise intolerance, lactic acidosis, and ragged-red fibers." | 1.35 | Myoclonic epilepsy with ragged-red fibers without increased lactate levels. ( Kimura, S; Kosuge, H; Nakamura, K; Nomura, K; Ozasa, S, 2009) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (42.86) | 18.7374 |
| 1990's | 1 (14.29) | 18.2507 |
| 2000's | 2 (28.57) | 29.6817 |
| 2010's | 1 (14.29) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Tort, F | 1 |
| Ugarteburu, O | 1 |
| Torres, MA | 1 |
| García-Villoria, J | 1 |
| Girós, M | 1 |
| Ruiz, A | 1 |
| Ribes, A | 1 |
| Kimura, S | 1 |
| Ozasa, S | 1 |
| Nakamura, K | 1 |
| Nomura, K | 1 |
| Kosuge, H | 1 |
| Arpa, J | 1 |
| Cruz-Martínez, A | 1 |
| Campos, Y | 1 |
| Gutiérrez-Molina, M | 1 |
| García-Rio, F | 1 |
| Pérez-Conde, C | 1 |
| Martín, MA | 1 |
| Rubio, JC | 1 |
| Del Hoyo, P | 1 |
| Arpa-Fernández, A | 1 |
| Arenas, J | 1 |
| van Hellenberg Hubar, JL | 1 |
| Gabreëls, FJ | 1 |
| Ruitenbeek, W | 1 |
| Sengers, RC | 1 |
| Renier, WO | 1 |
| Thijssen, HO | 1 |
| ter Laak, HJ | 1 |
| Mukoyama, M | 1 |
| Kazui, H | 1 |
| Sunohara, N | 1 |
| Yoshida, M | 1 |
| Nonaka, I | 1 |
| Satoyoshi, E | 1 |
| Mizuno, Y | 1 |
| Ishiguro, K | 1 |
| Okamoto, K | 1 |
| Morimatsu, M | 1 |
| Hirai, S | 1 |
| Hopkins, LC | 1 |
| Rosing, HS | 1 |
| Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
|---|---|---|---|---|---|---|---|
| Nutritional Assessment in Patients Affected by Mitochondrial Cytopathy[NCT02375438] | 26 participants (Actual) | Observational | 2014-12-31 | Completed | |||
| [information is prepared from clinicaltrials.gov, extracted Sep-2024] | |||||||
2 reviews available for lactic acid and Benign Infantile Myoclonic Epilepsy
| Article | Year |
|---|---|
MELAS syndrome. Report of two patients, and comparison with data of 24 patients derived from the literature.
Topics: Biopsy; Child; Child, Preschool; Electroencephalography; Electromyography; Energy Metabolism; Enzyme | 1991 |
Myoclonus and mitochondrial myopathy.
Topics: Adolescent; Brain Diseases, Metabolic; Central Nervous System Diseases; Electroencephalography; Epil | 1986 |
5 other studies available for lactic acid and Benign Infantile Myoclonic Epilepsy
| Article | Year |
|---|---|
Lysine Restriction and Pyridoxal Phosphate Administration in a NADK2 Patient.
Topics: Child; Diet; Epilepsies, Myoclonic; Female; Homozygote; Humans; Hyperlysinemias; Lactic Acid; Lysine | 2016 |
Myoclonic epilepsy with ragged-red fibers without increased lactate levels.
Topics: Adolescent; Anticonvulsants; Diagnosis, Differential; DNA Mutational Analysis; DNA, Mitochondrial; E | 2009 |
Prevalence and progression of mitochondrial diseases: a study of 50 patients.
Topics: Adolescent; Adult; Age of Onset; Aged; Disease Progression; DNA, Mitochondrial; Electromyography; Ep | 2003 |
Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes with acanthocytosis: a clinicopathological study of a unique case.
Topics: Acanthocytes; Acidosis; Adult; Aphasia; Atrophy; Biopsy; Cerebellum; Cerebral Cortex; Cerebral Ventr | 1986 |
[A case of mitochondrial encephalomyopathy characterized by repeated stroke-like episodes].
Topics: Adult; Brain Diseases; Cerebrovascular Disorders; Electroencephalography; Epilepsies, Myoclonic; Hum | 1989 |