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Related Experiment Videos

[A case contribution to the Gardner syndrome].

E Spens

    Stomatologie Der DDR
    |January 1, 1979
    PubMed
    Summary

    Gardner syndrome presents with benign skin, bone, and connective tissue tumors, but intestinal polyps carry a high risk of malignant transformation, leading to a poor prognosis. This summary outlines key clinical features, particularly those in the maxillofacial region.

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    Area of Science:

    • Genetics
    • Oncology
    • Dermatology

    Background:

    • Gardner syndrome is a rare genetic disorder characterized by a distinct set of clinical manifestations.
    • It is an autosomal dominant condition, a variant of familial adenomatous polyposis (FAP).