Apert syndrome, also known as acrocephalosyndactyly type 1 (ACS1), is a rare genetic disorder that occurs when the bones in the skull fuse together sooner than normal. This prevents the head from ...

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 is a rare congenital disorder that happens to 1 in 65,000 to 200,000 births across the globe. It occurs when the baby is still in the womb, and affects the skull, face, and at times ...

Coniglio says he never viewed his condition as a crutch, and says he's living proof that other people with Apert Syndrome can become coaches as well. His goal is to become a head coach.