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Yes, Jacobsen syndrome can potentially be detected prenatally through genetic testing methods such as chorionic villus sampling (CVS) or amniocentesis, which analyze the fetus’s chromosomes for abnormalities. Non-invasive prenatal testing (NIPT) can also assess the risk of chromosomal conditions, although it may not specifically identify Jacobsen syndrome. Early ultrasounds may reveal certain physical anomalies associated with the condition, but definitive diagnosis typically requires genetic analysis.

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13h ago

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See link for information.


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