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Related Experiment Videos

[The coxopodopatellar syndrome].

P Morin, C Vielpeau, L Fournier

    Journal De Radiologie
    |June 1, 1985
    PubMed
    Summary
    This summary is machine-generated.

    Coxopodopatellar syndrome is a rare genetic disorder characterized by patellar hypoplasia, pelvic skeletal anomalies, and forefoot abnormalities. This study details fifteen cases within a single family, highlighting its unique presentation.

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    Area of Science:

    • Genetics
    • Orthopedics
    • Rare diseases

    Background:

    • Coxopodopatellar syndrome presents with a distinct triad of symptoms.
    • Understanding the genetic basis and phenotypic variability is crucial for diagnosis.