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

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'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 ...

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.

FREELAND, MI -- A boy who has faced challenge after challenge in his young life is trying to win money for his school's robotics team ahead of the statewide robotics competition this weekend at ...

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.