Since President Donald Trump took office, Utah has begun the process of asking the federal government for a waiver to implement work and reporting requirements for some Medicaid recipients.

Artificial intelligence can be used for good, but a recent trend from social media has started to take things a little too far. On platforms such as TikTok and Instagram, AI is utilizing features ...

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… ...

A Lowell man stands accused of negligent homicide in the death of his blind adopted daughter.David Charles Whitten, 73, was arrested on Friday, Jan. 3.David Whitten had adopted six disabled adults ...

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.

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 ...

A recent study revealed that 77.4% of Mexican adults older than 60 years are affected by metabolic syndrome, indicating a looming public health crisis.

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 rare genetic disorder that manifests as craniosynostosis, craniofacial and limb dysmorphic features. Mutations in fibroblast growth factor receptor 2 (FGFR2) gene account for ...