Causes of Apert Syndrome:- Apert syndrome is a rare genetic disorder caused by a mutation in the FGFR2 gene, which controls bone development.- This gene mutation disrupts the timing of bone fusion ...
Apert syndrome (AS) is a genetic disorder that involves deformities in the skull, face, and limbs. Also known as acrocephalosyndactyly, it is characterized by craniosynostosis (premature union of ...
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