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Related Experiment Videos

Multiple synostosis syndrome

J C Pedersen, J P Fryns, G Carpentier

    European Journal of Pediatrics
    |September 1, 1980
    PubMed
    Summary
    This summary is machine-generated.

    This case report details a 2-year-old girl with multiple synostosis syndrome, a rare condition characterized by bone fusions. The diagnosis was supported by distinctive facial features and hearing loss.

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    Area of Science:

    • Genetics and Developmental Biology
    • Pediatric Medicine
    • Skeletal Dysplasias

    Background:

    • Multiple synostosis syndrome is a rare skeletal dysplasia.
    • Characterized by premature fusion of multiple bones.
    • Often associated with distinctive facial features and developmental issues.