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

[Neuronal migration disorders. Radiological and clinical aspects]

W J Orderud1, O H Skjeldal, P Strømme

  • 1Nevroradiologisk seksjon, Røntgen-Radiumavdelingen, Rikshospitalet, Oslo.

Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke
|June 20, 1995
PubMed
Summary

Neuronal migration disorders cause congenital brain malformations. Magnetic resonance imaging (MRI) is key for diagnosis, often revealing associated epilepsy and cerebral palsy in affected individuals.

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

The investigation of inborn errors of metabolism as an underlying cause of idiopathic intellectual disability in adults in Norway.

European journal of neurology·2015
Same author

Brain derived neurotrophic factor (BDNF) and autism spectrum disorders (ASD) in childhood.

European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society·2015
Same author

X-linked congenital ptosis and associated intellectual disability, short stature, microcephaly, cleft palate, digital and genital abnormalities define novel Xq25q26 duplication syndrome.

Human genetics·2013
Same author

Automated spectral EEG analyses of premature infants during the first three days of life correlated with developmental outcomes at 24 months.

Neonatology·2013
Same author

Learning disabilities and language pathology in patients with galactosemia.

Logopedics, phoniatrics, vocology·2011
Same author

A translocation between Xq21.33 and 22q13.33 causes an intragenic SHANK3 deletion in a woman with Phelan-McDermid syndrome and hypergonadotropic hypogonadism.

American journal of medical genetics. Part A·2011

Area of Science:

  • Neuroscience
  • Developmental Biology
  • Radiology

Background:

  • Neuronal migration disorders are a group of congenital cerebral malformations occurring during early gestation.
  • These disorders encompass conditions such as agyria, pachygyria, schizencephaly, polymicrogyria, and heterotopic gray matter.

Observation:

  • Magnetic resonance imaging (MRI) is the primary diagnostic modality for identifying neuronal migration disorders.
  • These conditions are frequently linked with neurological deficits including epilepsy, psychomotor retardation, and cerebral palsy.

Findings:

  • The study reviews the radiologic and clinical features of six patients diagnosed with various types of neuronal migration disorders.
  • Detailed case discussions highlight the diverse presentations and diagnostic challenges.

Related Experiment Videos

Implications:

  • Early and accurate diagnosis via MRI is crucial for managing associated neurological conditions.
  • Understanding these disorders aids in predicting developmental outcomes and planning interventions for affected children.