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

Primary megalencephaly at birth and low intelligence level.

S Petersson1, N L Pedersen, M Schalling

  • 1Neurogenetics Unit, Center for Molecular Medicine, Karolinska Institute, Stockholm, Sweden.

Neurology
|October 16, 1999
PubMed
Summary

Primary megalencephaly (PMG) at birth is linked to lower intelligence but not to vision or hearing issues. This condition shows moderate heritability, with mothers and children sharing similar head sizes at birth.

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

Clostridium difficile infection and risk of Parkinson's disease: a Swedish population-based cohort study.

European journal of neurology·2020
Same author

Joint impact of common risk factors on incident dementia: A cohort study of the Swedish Twin Registry.

Journal of internal medicine·2020
Same author

Clinical osteoarthritis of the hip and knee and fall risk: The role of low physical functioning and pain medication.

Seminars in arthritis and rheumatism·2020
Same author

The CODATwins Project: The Current Status and Recent Findings of COllaborative Project of Development of Anthropometrical Measures in Twins.

Twin research and human genetics : the official journal of the International Society for Twin Studies·2019
Same author

An epigenome-wide association study meta-analysis of educational attainment.

Molecular psychiatry·2017
Same author

Genetic susceptibility to cardiovascular disease and risk of dementia.

Translational psychiatry·2017

Area of Science:

  • Pediatric Neurology
  • Developmental Biology
  • Genetics

Background:

  • Primary megalencephaly (PMG) is defined by head circumference above the 98th percentile, indicating brain enlargement not caused by disease.
  • Previous studies show conflicting associations between PMG and intelligence in children.
  • PMG may have a genetic component, with potential inheritance patterns observed in childhood and adulthood.

Purpose of the Study:

  • To investigate the relationship between primary megalencephaly at birth and psychosensory conditions.
  • To assess mother-child similarity for primary megalencephaly at birth.

Main Methods:

  • Utilized birth records of 144,273 boys, identifying 732 with PMG.
  • Linked PMG data with information on intelligence, mental retardation, and sensory impairments (vision, hearing).

Related Experiment Videos

  • Examined parent-offspring similarity for PMG in 13,585 mother-child pairs.
  • Main Results:

    • PMG at birth was significantly associated with a lower intelligence level (OR, 1.32).
    • No significant association was found between PMG and mental retardation (OR, 1.31), or vision/hearing impairments.
    • A moderate heritability of head circumference and PMG was indicated by mother-child similarity (r=0.14 for HC, OR=2.55 for PMG).

    Conclusions:

    • Primary megalencephaly at birth serves as a risk factor for reduced intelligence.
    • PMG is not associated with increased risk for vision or hearing impairments.
    • Head circumference and PMG exhibit moderate heritability, suggesting a multifactorial inheritance pattern.