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

Möbius' syndrome: features and etiology

R Ghabrial1, P Versace, G Kourt

  • 1Department of Ophthalmology, New Children's Hospital, Westmead, Australia.

Journal of Pediatric Ophthalmology and Strabismus
|December 16, 1998
PubMed
Summary

Möbius syndrome, a rare neurological disorder, presents with diverse clinical features. Pregnancy-related vascular events may contribute to some cases, highlighting the need for multidisciplinary assessment.

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

Vascular endothelial growth factor improves functional outcome and decreases secondary degeneration in experimental spinal cord contusion injury.

Neuroscience·2003
Same author

Carbohydrate deficient glycoprotein syndrome type I: a cause of cerebellar vermis hypoplasia.

Journal of paediatrics and child health·1998
Same author

Velo-cardio-facial and partial DiGeorge phenotype in a child with interstitial deletion at 10p13--implications for cytogenetics and molecular biology.

American journal of medical genetics·1996
Same author

Psychotherapy and the ethics of attention.

The Hastings Center report·1996
Same author

Metaphyseal dysplasia-Bellini type. Report of two cases.

La Radiologia medica·1995
Same author

"CATCH 22" sans cardiac anomaly, thymic hypoplasia, cleft palate, and hypocalcaemia: cAtch 22. A common result of 22q11 deficiency?

Journal of medical genetics·1994

Area of Science:

  • Neurology
  • Genetics
  • Ophthalmology

Background:

  • Möbius syndrome is a rare congenital disorder characterized by facial nerve paralysis and other cranial nerve deficits.
  • Understanding its etiology and clinical spectrum is crucial for diagnosis and management.

Purpose of the Study:

  • To review the clinical features and potential causes of Möbius syndrome.
  • To analyze cases from a specific pediatric hospital over a 30-year period (1963-1995).

Main Methods:

  • Retrospective chart review of all diagnosed Möbius syndrome patients.
  • Comprehensive assessment by a geneticist and pediatric ophthalmologist for each patient.

Main Results:

  • Identified patterns in systemic and ocular clinical manifestations.

Related Experiment Videos

  • Found that 43% of the 23 studied patients had a history of significant in utero events.
  • Conclusions:

    • Möbius syndrome necessitates a multidisciplinary team approach for thorough patient evaluation.
    • Suggests that significant vascular events during pregnancy could be a contributing factor to fetal brainstem vascular disruption in some cases.