Kategoriak: All - symptoms - treatment - genetics - diagnosis

arabera Valentina González 6 years ago

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sindrome de crouzon

Crouzon syndrome is a rare genetic disorder characterized by the premature fusion of certain skull bones, leading to an abnormal shape of the head and face. This condition falls under the category of craniosynostosis and is primarily caused by mutations in the FGFR2 gene.

sindrome de crouzon

sindrome de crouzon

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