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

[Hallermann-Streiff syndrome].

M Parlato, G Alessandrella, S Martino

    Archivio Stomatologico
    |July 1, 1989
    PubMed
    Summary
    This summary is machine-generated.

    Hallermann-Streiff syndrome is a rare branchial arch defect causing significant eye, dental, and craniofacial issues. Management requires a multidisciplinary approach involving restorative dentistry, orthodontics, and maxillofacial surgery.

    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

    Final outcomes of the SOFT and TEXT phase III trials in premenopausal hormone receptor-positive early breast cancer.

    Annals of oncology : official journal of the European Society for Medical Oncology·2026
    Same author

    Contact-free characterization of nuclear mechanics using correlative Brillouin-Raman Micro-Spectroscopy in living cells.

    Acta biomaterialia·2025
    Same author

    Genomic characterisation of hormone receptor-positive breast cancer arising in very young women.

    Annals of oncology : official journal of the European Society for Medical Oncology·2023
    Same author

    Increase in landslide activity after a low-magnitude earthquake as inferred from DInSAR interferometry.

    Scientific reports·2022
    Same author

    Widening the Neuroimaging Features of Adenosine Deaminase 2 Deficiency.

    AJNR. American journal of neuroradiology·2021
    Same author

    A comparison of the implementation of assertive community treatment in Melbourne and London.

    Acta neuropsychiatrica·2016
    Same journal

    [Periodontal disease in children].

    Archivio stomatologico·1990
    Same journal

    [Photography in orthodontics].

    Archivio stomatologico·1990
    Same journal

    [Emergency situations in dental offices. 5. Medico-legal aspects and insurance].

    Archivio stomatologico·1990
    Same journal

    [Differential anchorage in orthodontics: problems and clinical implications].

    Archivio stomatologico·1990
    Same journal

    [Changes in the strength of immune defense of the oral cavity in aging].

    Archivio stomatologico·1990
    Same journal

    [The use of a computer in analysis of orthodontic cases].

    Archivio stomatologico·1990
    See all related articles

    Area of Science:

    • Genetics and developmental biology
    • Craniofacial anomalies
    • Syndromic disorders

    Context:

    • Hallermann-Streiff syndrome (HSS) is a rare genetic disorder.
    • It presents as a second branchial arch defect.
    • HSS is characterized by distinct ophthalmologic, dental, and craniofacial anomalies.

    Purpose:

    • To highlight the complex management challenges of Hallermann-Streiff syndrome.
    • To emphasize the need for a multidisciplinary approach in treating HSS patients.
    • To inform restorative dentists, orthodontists, and maxillofacial surgeons about the implications of HSS.

    Summary:

    • Hallermann-Streiff syndrome involves a constellation of ocular, dental, and craniofacial abnormalities.
    • These anomalies pose significant challenges for restorative dental and orthodontic treatment planning.

    Related Experiment Videos

  • Maxillofacial surgery is often required to address the craniofacial deformities associated with HSS.

    • Impact:

    • Improved understanding of Hallermann-Streiff syndrome's multifaceted nature.
    • Enhanced collaboration among dental and surgical specialists for comprehensive patient care.
    • Better treatment outcomes for individuals affected by this rare syndrome.