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Robotic joint reconstruction offers patients faster recovery, less pain, and personalized outcomes—here’s how it’s reshaping ...
“Pedro Acosta underwent surgery for chronic compartment syndrome in his right forearm,” the statement reads. “The rider will remain under observation for 24 hours and is expected to return at the ...
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 ...
AARON Chalmers’ ex Talia Oatway has shared the emotional moment their son Oakley walked for the first time after his gruelling health battle. Oakley, two, has Apert Syndrome, a genetic disord… ...
Because Apert syndrome is so rare, ... One of the first major hurdles Claire had to clear as an infant was a 20-hour craniosynostosis surgery — the first of two cranial surgeries Claire has ...
The Apert syndrome corresponds to the acrocephalosyndactyly type I, and it is characterized by craniosynostosis with fusion of any suture of the cranium and/or of the skull base, associated with ...
GEORDIE Shore star Aaron Chalmers has shared an update on the health of his son, Oakley who has a serious health condition. The one-year-old was born with Apert Syndrome, a rare genetic disorder wh… ...
We have been here nearly 5 weeks now. Unfortunately with Apert Syndrome the operations don't always go to plan. Oakley had to have this surgery to help his brain, development and to protect the eyes." ...
Webbed digits can result from Apert syndrome, a rare genetic anomaly that affects the bones. The condition generally is due to a mutation (genetic change) occurring in the fetus rather than being ...
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.
Apert syndrome is a genetic condition, caused by a mutation (change) on a specific gene. Research has identified the affected gene as the Fibroblast Growth Factor Receptor 2 (FGFR2) gene.
She said Elijah sustained an infection from the surgery and developed a severe brain injury at just 18 months old. ... He was born with Apert syndrome, just like her.