Learn all about Apert Syndrome, its causes, symptoms, diagnosis methods, and treatment options to manage this rare genetic ...

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 ...

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. Thomas, whose disorder ...

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 ...

“This is my beautiful son Oakley Bleu, he was born with a rare genetic syndrome called Apert syndrome.” Going on to explain what the condition is, Talia wrote: “Apert syndrome causes the ...

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.

"Learn and adapt" is his motto. He's had to do that since he was little. He was born with Apert Syndrome. It is a birth defect that causes deformities to the skull, face, teeth and limbs.