Page last updated: 2024-10-20

taurine and Intellectual Disability

taurine has been researched along with Intellectual Disability in 10 studies

Intellectual Disability: Subnormal intellectual functioning which originates during the developmental period. This has multiple potential etiologies, including genetic defects and perinatal insults. Intelligence quotient (IQ) scores are commonly used to determine whether an individual has an intellectual disability. IQ scores between 70 and 79 are in the borderline range. Scores below 67 are in the disabled range. (from Joynt, Clinical Neurology, 1992, Ch55, p28)

Research Excerpts

ExcerptRelevanceReference
"The Fragile X syndrome, a common form of mental retardation in humans, is caused by silencing the fragile X mental retardation (FMR1) gene leading to the absence of the encoded fragile X mental retardation protein 1 (FMRP)."1.31Alterations of amino acids and monoamine metabolism in male Fmr1 knockout mice: a putative animal model of the human fragile X mental retardation syndrome. ( Braun, K; Gruss, M, 2001)

Research

Studies (10)

TimeframeStudies, this research(%)All Research%
pre-19909 (90.00)18.7374
1990's0 (0.00)18.2507
2000's1 (10.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
GORDON, N1
WILSON, VK1
DINGMAN, HF1
WRIGHT, SW1
Gruss, M1
Braun, K1
Nalini, K1
Aroor, AR1
Rao, A1
Jacobsen, JG1
Smith, LH1
Crawhall, JC2
Purkiss, P2
Stanbury, JB2
Bir, K1
Ekelund, H1
Gamstorp, I1
Von Studnitz, W1
Mann, TP1
Dunn, HG1
Perry, TL1
Dolman, CL1

Reviews

1 review available for taurine and Intellectual Disability

ArticleYear
Biochemistry and physiology of taurine and taurine derivatives.
    Physiological reviews, 1968, Volume: 48, Issue:2

    Topics: Animals; Bile Acids and Salts; Chemical Phenomena; Chemistry; Female; Humans; In Vitro Techniques; I

1968

Other Studies

9 other studies available for taurine and Intellectual Disability

ArticleYear
ABNORMAL AMINO-ACID EXCRETION IN CEREBRAL DISEASE.
    Developmental medicine and child neurology, 1963, Volume: 5

    Topics: Brain Diseases; Cerebrospinal Fluid; Child; Chromatography; Cystine; Epilepsy; Glutamates; Humans; I

1963
A MULTIVARIATE ANALYSIS OF AMINO-ACID EXCRETIONS.
    Journal of mental deficiency research, 1964, Volume: 8

    Topics: Alanine; Amino Acid Metabolism, Inborn Errors; Amino Acids; Biomedical Research; Child; Chromatograp

1964
Alterations of amino acids and monoamine metabolism in male Fmr1 knockout mice: a putative animal model of the human fragile X mental retardation syndrome.
    Neural plasticity, 2001, Volume: 8, Issue:4

    Topics: 3,4-Dihydroxyphenylacetic Acid; Aging; Alanine; Amino Acids; Animals; Aspartic Acid; Brain; Brain St

2001
Urinary levels of taurine in mentally retarded children.
    Journal of mental deficiency research, 1989, Volume: 33 ( Pt 3)

    Topics: Adolescent; Cerebral Palsy; Child; Down Syndrome; Female; Humans; Intellectual Disability; Male; Mic

1989
Metabolism of sulfur-containing amino acids in a patient excreting -mercaptolactate-cysteine disulfide.
    Biochemical medicine, 1973, Volume: 7, Issue:1

    Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Autoanalysis; Carbon Isotopes; Cysteine; Cystine;

1973
Sulfur amino acids as precursors of beta-mercaptolactate-cysteine disulfide in human subjects.
    Biochemical medicine, 1971, Volume: 5, Issue:2

    Topics: Adult; Anilides; Cysteine; Diet; Dietary Proteins; Disulfides; Electrophoresis; Female; Humans; Inte

1971
Apparent response of impaired mental development, minor motor epilepsy and ataxia to pyridoxine.
    Acta paediatrica Scandinavica, 1969, Volume: 58, Issue:6

    Topics: Amino Acid Metabolism, Inborn Errors; Ataxia; Child; Child, Preschool; Electroencephalography; Epile

1969
Mental retardation, abnormal hair and mild aminoaciduria, all of unknown aetiology, in siblings.
    Proceedings of the Royal Society of Medicine, 1969, Volume: 62, Issue:4

    Topics: Alanine; Child, Preschool; Female; Fluoroscopy; Glutamine; Glycine; Hair; Humans; Intellectual Disab

1969
Homocystinuria. A recently discovered cause of mental defect and cerebrovascular thrombosis.
    Neurology, 1966, Volume: 16, Issue:4

    Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Animals; Blood; Blood Coagulation Disorders

1966