29 окт. 2020 г. · Apert syndrome is a type of syndromic craniosynostosis, and patients usually require one or more cranial and facial surgeries. In comparison ...

Craniofacial anomalies in Apert Syndrome may necessitate early surgical intervention in order to enable proper brain growth.

In Apert syndrome, both coronal sutures fuse before birth, leading to the skull being short from front to back but wide from side to side. Other sutures may ...

Apert syndrome, also known as acrocephalosyndactyly, is a genetic disorder that causes fusion of the skull, hands, and feet bones.

Apert syndrome is another genetically inherited syndrome characterized by craniosynostosis (premature fusion of coronal sutures) resulting in skull and ...

Apert syndrome is a rare genetic form of craniosynostosis — the early closing of 1 or more of the soft, fibrous seams between the skull bones (sutures). What is Apert syndrome? · Diagnosing Apert Syndrome

Apert syndrome is a rare genetic disorder characterized by the premature fusion of certain skull bones, leading to distinctive facial features and fused ...

The aim of this study was to review the outcomes of craniofacial and neurosurgical interventions in Apert syndrome patients treated at a single institution.

There are three basic operations used to bring the midface forward in Apert syndrome: the LeFort I, the LeFort III and the monobloc. The LeFort I brings the ...