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4. Causes of Cornelia de Lange Syndrome

A mutation in the NIPBL, SMC1A, HDAC8, RAD21, or SMC3 gene causes Cornelia de Lange syndrome. These genes produce a protein instrumental in fetal development called cohesin complex, and the mutation leads to abnormal production of the protein, resulting in impaired regulation and organization during development.

Cornelia de Lange causes genes mutations from2015 / Getty Images

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