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

[Gardner syndrome. Case reports].

Ferenc Koppány1, Arpád Joób-Fancsaly, Levente Pataky

  • 1Semmelweis Orvostudományi Egyetem, Szájsebészeti és Fogászati Klinika.

Fogorvosi Szemle
|March 13, 2003
PubMed
Summary

Gardner syndrome involves intestinal polyposis, osteomas, and skin tumors. Early dental or mandibular lesions can indicate this condition, prompting investigation for malignant polyposis.

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

Clinical Outcomes Associated with a Propolis-Based Nano-Formulated Bioadhesive Oral Gel: A Retrospective Case Series and Non-Randomized Controlled Study in Patients with Intellectual Disabilities.

Gels (Basel, Switzerland)·2026
Same author

Risk factors for the emergence of multidrug-resistant bacteria in patients with head and neck infections: a retrospective analysis.

Frontiers in oral health·2026
Same author

Clinical Applications and Therapeutic Potential of Nano-Bio Fusion Gel in Oral Soft Tissue Therapy: A Critical Narrative Review.

Gels (Basel, Switzerland)·2026
Same author

[Interdisciplinary consensus on the prevention of antiresorptive medication-related osteonecrosis of the jaw].

Orvosi hetilap·2026
Same author

Evaluating calcineurin inhibitors as alternatives to steroids in treating Oral Lichen Planus: a systematic review and meta-analysis.

Frontiers in oral health·2026
Same author

Comparative Safety and Efficacy of Patient-Specific Versus Hand-Molded Implants in Cranioplasty: A Systematic Review and Meta-Analysis.

Journal of clinical medicine·2025

Area of Science:

  • Medical Genetics
  • Oncology
  • Dentistry

Background:

  • Gardner syndrome is an inherited disorder characterized by familial adenomatous polyposis (FAP).
  • It presents with extracolonic manifestations including osteomas and skin tumors.
  • Early diagnosis is crucial due to the high risk of colorectal cancer.

Observation:

  • This report details three cases of Gardner syndrome.
  • Key features observed were malignant large intestine polyposis, multiple osteomas, and various skin tumors.
  • Dental and/or mandibular lesions were noted as the earliest presenting symptoms.

Findings:

  • The study highlights the diagnostic significance of dental and mandibular abnormalities in suspecting Gardner syndrome.
  • Malignant polyposis of the large intestine is a primary concern in affected individuals.

Related Experiment Videos

  • The combination of polyposis, osteomas, and skin tumors defines the syndrome's presentation.

    • Implications:

    • Recognizing early dental signs can lead to timely diagnosis of Gardner syndrome.
    • Prompt identification facilitates management of colorectal cancer risk.
    • This underscores the interdisciplinary approach needed for managing rare genetic syndromes.