Apert's syndrome is caused by a spontaneous mutation or passed down from a parent with the disease. The likelihood of the diagnosis is one in 200,000. "They have to undergo multiple surgeries, they ...

Apert's Syndrome: Why Kids Of Older Dads Are More Likely To Have Some Genetic Disorders Date: July 15, 2008 Source: University of Southern California ...

Learn about Apert syndrome, a genetic condition that causes abnormal head, hand, and foot development. We look at symptoms, treatment, and outlook.

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.

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 ...

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, ...

Apert syndrome almost always results from new genetic changes (mutations) that occur randomly. People with Apert syndrome can undergo therapies that address specific symptoms.