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[Ivemark's syndrome (author's transl)]

M Reuss, D Wilker

    Zeitschrift Fur Kardiologie
    |July 1, 1980
    PubMed
    Summary
    This summary is machine-generated.

    Ivemark's syndrome, a congenital heart defect with asplenia, arises from embryonic factors. Early diagnosis via imaging and blood tests is crucial due to high mortality.

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    Area of Science:

    • Embryology
    • Cardiovascular Science
    • Genetics

    Background:

    • Ivemark's syndrome, also known as asplenia, is a rare congenital disorder.
    • It involves complex congenital heart disease and abnormal visceral organ arrangement.
    • The condition is associated with the absence of the spleen (asplenia).

    Observation:

    • Presents a case report of a newborn diagnosed with Ivemark's syndrome.
    • Details the etiology, embryology, and anatomy of this condition.
    • Highlights associated visceral abnormalities.

    Findings:

    • The disorder stems from an exogenous or endogenous factor affecting embryonic development between days 28-32.
    • High lethality rates are observed, regardless of surgical intervention.

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  • Early clinical diagnosis is recommended.

    • Implications:

    • Suggests diagnostic methods including X-ray, blood smear, ultrasound, and angiocardiography.
    • Emphasizes the importance of timely diagnosis for potential intervention.
    • Underscores the critical need for understanding embryological development in congenital diseases.