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 ...

Apert Syndrome: Causes, Symptoms, Diagnosis and Treatment: By Shreoshree Chakrabarty Apert syndrome is a rare genetic condition that impacts the normal development of the skull, leading to an ...

Apert syndrome is a condition where the skull fuses prematurely, said Dr. John Meara, one of the physicians at Boston Children’s Hospital who Cam sees regularly. “Most people think that in your head ...

Apert syndrome is a rare genetic disorder that causes a fetus’ facial and skull bones to fuse together too early in its development. Apert syndrome causes facial and skull abnormalities, which can ...