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methylmalonic acid and Brain Disorders

methylmalonic acid has been researched along with Brain Disorders in 9 studies

Methylmalonic Acid: A malonic acid derivative which is a vital intermediate in the metabolism of fat and protein. Abnormalities in methylmalonic acid metabolism lead to methylmalonic aciduria. This metabolic disease is attributed to a block in the enzymatic conversion of methylmalonyl CoA to succinyl CoA.
methylmalonic acid : A dicarboxylic acid that is malonic acid in which one of the methylene hydrogens is substituted by a methyl group.

Research Excerpts

ExcerptRelevanceReference
"The Cobalamin C deficiency (cblC), characterized with elevated methylmalonic acidemia and homocystinuria in plasma, is an inborn error of cobalamin metabolism."3.88Late-onset cobalamin C deficiency Chinese sibling patients with neuropsychiatric presentations. ( Liu, YM; Wang, SJ; Yan, CZ; Zhao, YY, 2018)
"Methylmalonic acidemia (MMA) is an autosomal-recessive inborn error of metabolism."2.44Methylmalonic acidemia: brain imaging findings in 52 children and a review of the literature. ( Ghanaati, H; Molaei, S; Radmanesh, A; Robertson, RL; Zaman, T; Zamani, AA, 2008)
"No methylmalonic acidemia has been reported in children with CDKL5 disorder."1.48A male case with CDKL5-associated encephalopathy manifesting transient methylmalonic acidemia. ( Akamine, S; Fukai, R; Hara, T; Ishizaki, Y; Kimura, M; Koga, H; Matsumoto, N; Miyake, N; Ohga, S; Ohkubo, K; Saitsu, H; Sakai, Y; Sakamoto, O; Sakata, A; Sanefuji, M; Torisu, H; Yamaguchi, S, 2018)
"We report the first case of acute encephalopathy induced by vaccination in an infant with methylmalonic aciduria cblA in China."1.42[Acute encephalopathy induced by vaccination in an infant with methylmalonic aciduria cblA]. ( Ding, Y; Li, X; Liu, Y; Song, J; Wang, H; Wang, Q; Wu, T; Yang, Y; Zhang, Y, 2015)
"A child was seen because of encephalopathy and metabolic ketoacidosis at 19 months."1.27Bilateral lucency of the globus pallidus complicating methylmalonic acidemia. ( Korf, B; Levy, HL; Wallman, JK, 1986)

Research

Studies (9)

TimeframeStudies, this research(%)All Research%
pre-19902 (22.22)18.7374
1990's3 (33.33)18.2507
2000's1 (11.11)29.6817
2010's3 (33.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Wang, SJ1
Yan, CZ1
Liu, YM1
Zhao, YY1
Akamine, S1
Ishizaki, Y1
Sakai, Y1
Torisu, H1
Fukai, R1
Miyake, N1
Ohkubo, K1
Koga, H1
Sanefuji, M1
Sakata, A1
Kimura, M1
Yamaguchi, S1
Sakamoto, O1
Hara, T1
Saitsu, H1
Matsumoto, N1
Ohga, S1
Liu, Y1
Wu, T1
Wang, H1
Ding, Y1
Song, J1
Li, X1
Zhang, Y1
Wang, Q1
Yang, Y1
Radmanesh, A1
Zaman, T1
Ghanaati, H1
Molaei, S1
Robertson, RL1
Zamani, AA1
Capece, G1
Giliberti, P1
Militerni, R1
Pignero, A1
Mayatepek, E1
Hoffmann, GF1
Baumgartner, R1
Schulze, A1
Jakobs, C1
Trefz, FK1
Bremer, HJ1
van Asselt, DZ1
Karlietis, MH1
Poels, PJ1
de Jong, JG1
Wevers, RA1
Hoefnagels, WH1
Vellema, P1
van den Ingh, TS1
Wouda, W1
Korf, B1
Wallman, JK1
Levy, HL1

Reviews

1 review available for methylmalonic acid and Brain Disorders

ArticleYear
Methylmalonic acidemia: brain imaging findings in 52 children and a review of the literature.
    Pediatric radiology, 2008, Volume: 38, Issue:10

    Topics: Amino Acid Metabolism, Inborn Errors; Brain Diseases; Child, Preschool; Female; Humans; Infant; Infa

2008

Trials

1 trial available for methylmalonic acid and Brain Disorders

ArticleYear
Pathological changes in cobalt-supplemented and non-supplemented twin lambs in relation to blood concentrations of methylmalonic acid and homocysteine.
    The veterinary quarterly, 1999, Volume: 21, Issue:3

    Topics: Animals; Brain; Brain Diseases; Cobalt; Copper; Diet; Female; Hepatitis, Chronic; Homocysteine; Litt

1999

Other Studies

7 other studies available for methylmalonic acid and Brain Disorders

ArticleYear
Late-onset cobalamin C deficiency Chinese sibling patients with neuropsychiatric presentations.
    Metabolic brain disease, 2018, Volume: 33, Issue:3

    Topics: Adolescent; Adult; Asian People; Atrophy; Brain; Brain Diseases; Carrier Proteins; Child; Child, Pre

2018
A male case with CDKL5-associated encephalopathy manifesting transient methylmalonic acidemia.
    European journal of medical genetics, 2018, Volume: 61, Issue:8

    Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Brain Diseases; Humans; Male; Methionine; Methylma

2018
[Acute encephalopathy induced by vaccination in an infant with methylmalonic aciduria cblA].
    Zhonghua er ke za zhi = Chinese journal of pediatrics, 2015, Volume: 53, Issue:1

    Topics: Amino Acid Metabolism, Inborn Errors; Brain Diseases; Carnitine; Diet, Protein-Restricted; Hepatitis

2015
[A case of metabolic encephalopathy caused by vitamin B 12-dependent methylmalonicaciduria].
    Acta neurologica. Quaderni, 1981, Volume: 42

    Topics: Amino Acid Metabolism, Inborn Errors; Brain Diseases; Female; Humans; Infant; Malonates; Methylmalon

1981
Atypical vitamin B12-unresponsive methylmalonic aciduria in sibship with severe progressive encephalomyelopathy: a new genetic disease?
    European journal of pediatrics, 1996, Volume: 155, Issue:5

    Topics: Amino Acid Metabolism, Inborn Errors; Brain Diseases; Child; Child, Preschool; Disease Progression;

1996
Cerebrospinal fluid methylmalonic acid concentrations in neurological patients with low and normal serum cobalamin concentrations.
    Acta neurologica Scandinavica, 1998, Volume: 97, Issue:6

    Topics: Adult; Aged; Brain Diseases; Female; Humans; Male; Mental Disorders; Methylmalonic Acid; Middle Aged

1998
Bilateral lucency of the globus pallidus complicating methylmalonic acidemia.
    Annals of neurology, 1986, Volume: 20, Issue:3

    Topics: Brain Diseases; Female; Globus Pallidus; Humans; Infant; Malonates; Methylmalonic Acid; Tomography,

1986