Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

DOes the child with a learning disability have a biochemical defect?

P M Leary

    South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde
    |January 2, 1982
    PubMed
    Summary

    Neurobiochemical research suggests a potential catecholamine metabolism defect in some children with learning disabilities, possibly linked to genetics. This hypothesis, while heuristic, offers insights into underarousal and stimulant response in this heterogeneous group.

    Related Concept Videos

    You might also read

    Related Articles

    Articles linked to this work by shared authors, journal, and citation graph.

    Sort by
    Same author

    Conversion disorder.

    Handbook of clinical neurology·2013
    Same author

    Conversion disorder in childhood--diagnosed too late, investigated too much?

    Journal of the Royal Society of Medicine·2003
    Same author

    Childhood secondary (symptomatic) epilepsy, seizure control, and intellectual handicap in a nontropical region of South Africa.

    Epilepsia·1999
    Same author

    Case report and molecular analysis of subacute sclerosing panencephalitis in a South African Child.

    Journal of clinical microbiology·1999
    Same author

    'Botulinum toxin treatment in cerebral palsy: intervention with poor evaluation?'.

    Developmental medicine and child neurology·1999
    Same author

    Interventions for children with neurodevelopmental delay.

    South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde·1998

    Area of Science:

    • Neurobiology
    • Developmental Psychology
    • Genetics

    Background:

    • Learning disabilities in children lack direct brain study access, necessitating hypothetical neurobiochemical explanations.
    • Catecholamines, including noradrenaline and dopamine, are crucial for mood, emotion, and arousal regulation in the brain.

    Purpose of the Study:

    • To explore the hypothetical neurobiochemical basis of learning disabilities, focusing on catecholamine metabolism.
    • To investigate the potential role of catecholamine dysfunction in underarousal and stimulant medication response observed in some learning-disabled children.

    Main Methods:

    • Review of physiological evidence of underarousal in learning-disabled children.
    • Analysis of the effects of stimulant medication.
    • Examination of pathological and comparative neurochemical studies.

    Related Experiment Videos

  • Consideration of familial clustering patterns.
  • Main Results:

    • Physiological data and stimulant response suggest a possible defect in catecholamine metabolism in some learning-disabled children.
    • Pathological and neurochemical studies offer support for the catecholamine hypothesis.
    • Familial clustering indicates a potential underlying genetic mechanism for the biochemical defect.

    Conclusions:

    • A neurobiochemical model positing a defect in catecholamine metabolism is a heuristic explanation for some learning disabilities.
    • This model is not universally applicable due to the heterogeneity of learning-disabled children.
    • Further research is needed to understand the complex neurobiology of learning disabilities.