Apert syndrome symptoms typically become apparent at birth and can include a high forehead, wide-set eyes, and an underdeveloped midface. Although there is no permanent cure, ...

She was born in 1968 with Apert syndrome, which causes the fusion of bones in the feet, hands and skull. At just days old, doctors said she wouldn’t live a normal life.

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 ...

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 ...

What is Apert syndrome as Geordie Shore’s Aaron Chalmers shares son’s heartbreaking diagnosis. As Aaron Chalmers' ex-girlfriend Talia Oatway shares the first photos of their son, ...

Flor is a former KENS 5 employee, and as colleagues, we have helped raise awareness of her daughter, Mirlee's, condition, Apert Syndrome. It's a condition that causes the fusion of bones in the ...

MADISONVILLE, Texas (KBTX) - The Madisonville Consolidated Independent School District hosted a volleyball tournament to support Waylon, a one-year-old facing the challenges of Apert Syndrome.

He was born with Apert Syndrome. It is a birth defect that causes deformities to the skull, face, teeth and limbs. "When I was born my fingers were stuck together," Coniglio said.