lactic acid has been researched along with Spasms, Infantile in 10 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.
Spasms, Infantile: An epileptic syndrome characterized by the triad of infantile spasms, hypsarrhythmia, and arrest of psychomotor development at seizure onset. The majority present between 3-12 months of age, with spasms consisting of combinations of brief flexor or extensor movements of the head, trunk, and limbs. The condition is divided into two forms: cryptogenic (idiopathic) and symptomatic (secondary to a known disease process such as intrauterine infections; nervous system abnormalities; BRAIN DISEASES, METABOLIC, INBORN; prematurity; perinatal asphyxia; TUBEROUS SCLEROSIS; etc.). (From Menkes, Textbook of Child Neurology, 5th ed, pp744-8)
| Excerpt | Relevance | Reference |
|---|---|---|
| " This broadens the differential diagnosis of D-lactic acidosis, an increasingly recognized complication of short bowel syndrome with unpredictable onset and severity." | 3.91 | Identification of human D lactate dehydrogenase deficiency. ( Bakkers, J; Bosco, P; Calì, F; de Koning, TJ; de Sain-van der Velden, MGM; Duran, KJ; Duran, M; Fuchs, SA; Geleijns, K; Gerrits, J; Jans, JJ; Knoers, NV; Koot, BG; Lichtenbelt, KD; Monroe, GR; Oostendorp, M; Savelberg, SMC; Terhal, PA; Tessadori, F; van Aalderen, M; van Alfen, JC; van der Crabben, SN; van Eerde, AM; van Gassen, KL; van Haaften, G; van Roosmalen, MJ; Verhoeven-Duif, NM; Visser, G, 2019) |
| "We treated a female patient with West syndrome caused by thiamine-responsive pyruvate dehydrogenase complex (PDHC) deficiency." | 2.40 | Concomitant administration of sodium dichloroacetate and thiamine in west syndrome caused by thiamine-responsive pyruvate dehydrogenase complex deficiency. ( Chen, S; Ito, M; Kuroda, Y; Maehara, M; Naito, E; Saijo, T; Yokota, I, 1999) |
| "PEHO syndrome is a rare symptom complex of severe progressive encephalopathy, edema, hypsarrhythmia, and optic atrophy." | 1.33 | Serial MR imaging, diffusion tensor imaging, and MR spectroscopic findings in a child with progressive encephalopathy, edema, hypsarrhythmia, and optic atrophy (PEHO) syndrome. ( Boltshauser, E; Huisman, TA; Klein, A; Straube, T; Werner, B, 2006) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 4 (40.00) | 18.2507 |
| 2000's | 4 (40.00) | 29.6817 |
| 2010's | 2 (20.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Monroe, GR | 1 |
| van Eerde, AM | 1 |
| Tessadori, F | 1 |
| Duran, KJ | 1 |
| Savelberg, SMC | 1 |
| van Alfen, JC | 1 |
| Terhal, PA | 1 |
| van der Crabben, SN | 1 |
| Lichtenbelt, KD | 1 |
| Fuchs, SA | 1 |
| Gerrits, J | 1 |
| van Roosmalen, MJ | 1 |
| van Gassen, KL | 1 |
| van Aalderen, M | 1 |
| Koot, BG | 1 |
| Oostendorp, M | 1 |
| Duran, M | 1 |
| Visser, G | 1 |
| de Koning, TJ | 1 |
| Calì, F | 1 |
| Bosco, P | 1 |
| Geleijns, K | 1 |
| de Sain-van der Velden, MGM | 1 |
| Knoers, NV | 1 |
| Bakkers, J | 1 |
| Verhoeven-Duif, NM | 1 |
| van Haaften, G | 1 |
| Jans, JJ | 1 |
| Cassandrini, D | 1 |
| Cilio, MR | 1 |
| Bianchi, M | 1 |
| Doimo, M | 1 |
| Balestri, M | 1 |
| Tessa, A | 1 |
| Rizza, T | 1 |
| Sartori, G | 1 |
| Meschini, MC | 1 |
| Nesti, C | 1 |
| Tozzi, G | 1 |
| Petruzzella, V | 1 |
| Piemonte, F | 1 |
| Bisceglia, L | 1 |
| Bruno, C | 1 |
| Dionisi-Vici, C | 1 |
| D'Amico, A | 1 |
| Fattori, F | 1 |
| Carrozzo, R | 1 |
| Salviati, L | 1 |
| Santorelli, FM | 1 |
| Bertini, E | 1 |
| Shah, NS | 1 |
| Mitchell, WG | 1 |
| Boles, RG | 1 |
| Huisman, TA | 1 |
| Klein, A | 1 |
| Werner, B | 1 |
| Straube, T | 1 |
| Boltshauser, E | 1 |
| Azzopardi, D | 1 |
| Edwards, D | 1 |
| Bakker, HD | 1 |
| Van den Bogert, C | 1 |
| Drewes, JG | 1 |
| Barth, PG | 1 |
| Scholte, HR | 1 |
| Wanders, RJ | 1 |
| Ruitenbeek, W | 1 |
| Naito, E | 1 |
| Ito, M | 2 |
| Yokota, I | 1 |
| Saijo, T | 1 |
| Chen, S | 1 |
| Maehara, M | 1 |
| Kuroda, Y | 2 |
| Sfaello, I | 1 |
| Castelnau, P | 1 |
| Blanc, N | 1 |
| Ogier, H | 1 |
| Evrard, P | 1 |
| Arzimanoglou, A | 1 |
| Giordano, G | 1 |
| Corradi, D | 1 |
| D'Adda, T | 1 |
| Melissari, M | 1 |
| Miyazaki, M | 1 |
| Hashimoto, T | 1 |
| Murakawa, K | 1 |
| Tayama, M | 1 |
2 reviews available for lactic acid and Spasms, Infantile
| Article | Year |
|---|---|
Magnetic resonance spectroscopy in neonates.
Topics: Adult; Aspartic Acid; Asphyxia Neonatorum; Brain; Energy Metabolism; Humans; Infant; Infant, Newborn | 1995 |
Concomitant administration of sodium dichloroacetate and thiamine in west syndrome caused by thiamine-responsive pyruvate dehydrogenase complex deficiency.
Topics: Amino Acid Substitution; Dichloroacetic Acid; DNA Mutational Analysis; Drug Therapy, Combination; Fe | 1999 |
8 other studies available for lactic acid and Spasms, Infantile
| Article | Year |
|---|---|
Identification of human D lactate dehydrogenase deficiency.
Topics: Acidosis, Lactic; Adult; Animals; Consanguinity; Diagnosis, Differential; Homozygote; Humans; Infant | 2019 |
Pontocerebellar hypoplasia type 6 caused by mutations in RARS2: definition of the clinical spectrum and molecular findings in five patients.
Topics: Arginine-tRNA Ligase; Cerebellum; Child, Preschool; Female; Follow-Up Studies; Humans; Infant; Infan | 2013 |
Mitochondrial disorders: a potentially under-recognized etiology of infantile spasms.
Topics: Diagnosis, Differential; DNA, Mitochondrial; Energy Metabolism; Female; Humans; Infant; Infant, Newb | 2002 |
Serial MR imaging, diffusion tensor imaging, and MR spectroscopic findings in a child with progressive encephalopathy, edema, hypsarrhythmia, and optic atrophy (PEHO) syndrome.
Topics: Aspartic Acid; Atrophy; Brain Diseases; Brain Edema; Cerebellum; Child; Choline; Creatine; Diffusion | 2006 |
Progressive generalized brain atrophy and infantile spasms associated with cytochrome c oxidase deficiency.
Topics: Acidosis; Atrophy; Brain; Cytochrome-c Oxidase Deficiency; Humans; Infant, Newborn; Lactates; Lactic | 1996 |
Infantile spasms and Menkes disease.
Topics: Brain; Ceruloplasmin; Copper; Electroencephalography; Histidine; Humans; Infant; Infant, Newborn; La | 2000 |
[An autopsy case of neonatal lactic acidosis].
Topics: Acidosis, Lactic; Atrophy; Autopsy; Body Fluids; Brain; Cardiomegaly; Epilepsy, Generalized; Fatal O | 2001 |
[Cerebral lactate and pyruvate metabolism in infantile spasms].
Topics: Adrenocorticotropic Hormone; Brain; Humans; Infant; Lactates; Lactic Acid; Male; Pyruvates; Pyruvic | 1992 |