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

Oculoauriculovertebral dysplasia (Goldenhar's syndrome).

A D Kallor, W M Hendricks

    Cutis
    |July 1, 1979
    PubMed
    Summary

    Oculoauriculovertebral dysplasia is a rare congenital disorder affecting the eyes, ears, and spine. This review details a case and literature, highlighting its complex presentation and associated anomalies.

    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

    What do eighth-grade students at South Asheboro Middle School know about basic health?

    North Carolina medical journal·1996
    Same author

    Protecting yourself from the sun. Are you allergic to your sunscreen?

    North Carolina medical journal·1995
    Same author

    Getting a great tan without damaging your skin. Artificial tanning products.

    North Carolina medical journal·1995
    Same author

    Histamine release in chronic idiopathic urticaria.

    The New England journal of medicine·1993
    Same author

    Pellagra and pellagralike dermatoses: etiology, differential diagnosis, dermatopathology, and treatment.

    Seminars in dermatology·1991
    Same author

    Wrinkles.

    North Carolina medical journal·1991

    Area of Science:

    • Genetics and Developmental Biology
    • Craniofacial and Skeletal Anomalies

    Background:

    • Oculoauriculovertebral dysplasia (OAVD), also known as Goldenhar syndrome, is a complex congenital disorder.
    • It is characterized by a spectrum of anomalies affecting the first branchial arch derivatives.

    Observation:

    • This report presents a specific case of OAVD.
    • The case illustrates the typical triad of epibulbar dermoids, preauricular appendages/fistulae, and vertebral anomalies.

    Findings:

    • The syndrome is associated with a wide range of other congenital malformations.
    • Review of literature confirms the variable expressivity and frequent co-occurrence of anomalies.

    Implications:

    • Understanding OAVD is crucial for accurate diagnosis and genetic counseling.
    • Further research into the etiology and management of OAVD is warranted.

    Related Experiment Videos