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

Craniometaphyseal dysplasia

F W Martin

    The Journal of Laryngology and Otology
    |February 1, 1977
    PubMed
    Summary

    This case report details craniometaphyseal dysplasia, a rare bone disorder. It highlights unusual symptoms like facial paresis and mastoid surgery, with no further patient decline observed.

    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

    Re: Wedge resection & modified mattress suture for correcting anterior septal deviation: how we do it.

    Clinical otolaryngology : official journal of ENT-UK ; official journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery·2012
    Same author

    The effect of FloSeal on post-tonsillectomy pain: a randomised controlled pilot study.

    Clinical otolaryngology : official journal of ENT-UK ; official journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery·2008
    Same author

    Departmental audit of tonsillectomy haemorrhage rates: pitfalls in interpretation.

    The Journal of laryngology and otology·2006
    Same author

    Audit of stapedectomy results in a district general hospital.

    Clinical otolaryngology and allied sciences·2002
    Same author

    Trans-nasal endoscopic holmium: YAG laser correction of choanal atresia.

    The Journal of laryngology and otology·1996
    Same author

    Unusual presentation of verrucous carcinoma of maxillary antrum.

    The Journal of otolaryngology·1992

    Area of Science:

    • Medical Science
    • Genetics
    • Orthopedics

    Background:

    • Craniometaphyseal dysplasia is a rare autosomal dominant disorder characterized by progressive bone obliteration, primarily affecting the craniofacial and long bones.
    • Literature review supports classification and understanding of this skeletal dysplasia.
    • This condition requires comprehensive diagnostic and management strategies.

    Observation:

    • Presentation of a unique case of craniometaphyseal dysplasia.
    • Observed unusual clinical features including prior mastoid surgery and subsequent contralateral temporary facial paresis.
    • Patient's condition remained stable without symptom progression during follow-up.

    Findings:

    • The case report contributes to the classification of craniometaphyseal dysplasia.
    • Highlights the importance of recognizing atypical presentations and potential complications.
    • Demonstrates a stable disease course in this specific patient post-intervention.

    Implications:

    • Enhances understanding of craniometaphyseal dysplasia's diverse clinical spectrum.
    • Informs clinical practice regarding the management of rare skeletal dysplasias.
    • Suggests the need for vigilant monitoring and tailored treatment approaches for affected individuals.

    Related Experiment Videos