What is a common craniofacial feature associated with Apert Syndrome?

Apert Syndrome is characterized by various craniofacial and limb malformations, one of the most notable features being syndactyly, which is the fusion or webbing of fingers and/or toes. This condition results from abnormal development during the early stages of embryogenesis, particularly affecting the development of the limbs.

The syndactyly often affects both the hands and feet, leading to a distinctive physical presentation that is recognized as a hallmark of the syndrome. Understanding the implications of syndactyly in Apert Syndrome is crucial, as it can influence surgical planning for correction and overall patient management.

Other prominent features of Apert Syndrome include craniosynostosis and facial deformities, but the option regarding syndactyly directly relates to limb abnormalities, making it the most relevant answer to this question.