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craniosynostosis

Image shows a 3d representation of a baby's skull.

Featured Genetics Neurology

·September 8, 2016·5 min read

Rare and Common Genetic Variants Combine to Cause Skull Fusion Disorder

Researchers have identified genetic mutations they believe are responsible for midline craniosynostosis.

This shows a DNA double helix

Featured Genetics Neurology Neuroscience Open Neuroscience Articles

·July 1, 2019·3 min read

Researchers discover genetic mutation behind serious skull disorder

A mutation in the BCL11B gene appears to be responsible for a rare skull development disorder called craniosynostosis.