Page last updated: 2024-10-17

lactic acid and Chronic Progressive External Ophthalmoplegia with Myopathy

lactic acid has been researched along with Chronic Progressive External Ophthalmoplegia with Myopathy 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.

Research Excerpts

ExcerptRelevanceReference
" Among them, there were 19 cases of mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS), 2 cases of encephalopathies which could not be classified into any specific type, 2 cases of floppy infants, one case of Kearns-Sayer syndrome (KSS) and one case of mitochondrial entero-myopathy."3.73[Phenotype heterogeneity associated with mitochondrial DNA A3243G mutation]. ( Niu, SL; Pei, P; Qi, Y; Wang, ZX; Xu, YF; Yang, YL; Yuan, Y; Zhang, Y, 2005)
"Localized brain proton MR spectra were acquired from patients with different mitochondrial encephalomyopathies (myoclonus epilepsy with ragged-red fibers [MERRF], Kearns-Sayre syndrome [KSS], and mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes [MELAS])."3.68Proton MR spectroscopic characterization of differences in regional brain metabolic abnormalities in mitochondrial encephalomyopathies. ( Andermann, F; Arnold, DL; Karpati, G; Mathews, PM; Silver, K, 1993)

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19901 (14.29)18.7374
1990's3 (42.86)18.2507
2000's2 (28.57)29.6817
2010's1 (14.29)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Semeraro, M1
Boenzi, S1
Carrozzo, R1
Diodato, D1
Martinelli, D1
Olivieri, G1
Antonetti, G1
Sacchetti, E1
Catesini, G1
Rizzo, C1
Dionisi-Vici, C1
Zhang, Y1
Wang, ZX1
Niu, SL1
Xu, YF1
Pei, P1
Yuan, Y1
Yang, YL1
Qi, Y1
Berio, A1
Piazzi, A1
Kuwabara, T1
Watanabe, H1
Tanaka, K1
Tsuji, S1
Ohkubo, M1
Ito, T1
Sakai, K1
Yuasa, T1
Mathews, PM1
Andermann, F1
Silver, K1
Karpati, G1
Arnold, DL1
Choi, C1
Sunwoo, IN1
Kim, HS1
Kim, DI1
Furuya, H1
Motomura, S1
Kitaguchi, T1
Ishimoto, S1
Goto, I1

Other Studies

7 other studies available for lactic acid and Chronic Progressive External Ophthalmoplegia with Myopathy

ArticleYear
The urinary organic acids profile in single large-scale mitochondrial DNA deletion disorders.
    Clinica chimica acta; international journal of clinical chemistry, 2018, Volume: 481

    Topics: 3-Hydroxybutyric Acid; Acyl-CoA Dehydrogenase, Long-Chain; Adolescent; Child; Child, Preschool; Cong

2018
[Phenotype heterogeneity associated with mitochondrial DNA A3243G mutation].
    Zhongguo yi xue ke xue yuan xue bao. Acta Academiae Medicinae Sinicae, 2005, Volume: 27, Issue:1

    Topics: Adolescent; Adult; Child; Child, Preschool; DNA, Mitochondrial; Female; Humans; Infant; Kearns-Sayre

2005
Improvement of Kearns-Sayre syndrome with controlled carbohydrate intake and coenzyme Q10 therapy.
    Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde, 1994, Volume: 208, Issue:6

    Topics: Child; Coenzymes; Combined Modality Therapy; Dietary Carbohydrates; Humans; Kearns-Sayre Syndrome; L

1994
Mitochondrial encephalomyopathy: elevated visual cortex lactate unresponsive to photic stimulation--a localized 1H-MRS study.
    Neurology, 1994, Volume: 44, Issue:3 Pt 1

    Topics: Humans; Kearns-Sayre Syndrome; Lactates; Lactic Acid; Magnetic Resonance Imaging; Magnetic Resonance

1994
Proton MR spectroscopic characterization of differences in regional brain metabolic abnormalities in mitochondrial encephalomyopathies.
    Neurology, 1993, Volume: 43, Issue:12

    Topics: Aspartic Acid; Brain; Choline; Creatine; Humans; Kearns-Sayre Syndrome; Lactates; Lactic Acid; Magne

1993
Transient improvement of pyruvate metabolism after coenzyme Q therapy in Kearns-Sayre syndrome: MRS study.
    Yonsei medical journal, 2000, Volume: 41, Issue:5

    Topics: Adolescent; Brain; Female; Humans; Kearns-Sayre Syndrome; Lactic Acid; Magnetic Resonance Spectrosco

2000
[A case of Kearns-Sayre-Shy syndrome with neuropathy and high lactate content in CSF].
    Rinsho shinkeigaku = Clinical neurology, 1985, Volume: 25, Issue:10

    Topics: Humans; Kearns-Sayre Syndrome; Lactates; Lactic Acid; Male; Middle Aged; Ophthalmoplegia; Peripheral

1985