Walker Henry Schneller Brown is a child of modern medical science. Born with the rare genetic condition, cardiofaciocutaneous syndrome, he is medically complex and fragile and would not have survived ...

Walker suffers from cardiofaciocutaneous syndrome, or CFC, an extremely rare syndrome only a few dozen people in the world have.

He was born with an impossibly rare genetic mutation, cardiofaciocutaneous syndrome, a technical name for a mash of symptoms. He is globally delayed and can't speak, so I never know what's wrong.

Ian and Johanna Schneller’s son Walker was born with a rare genetic disorder, Cardiofaciocutaneous (CFC) syndrome. It made him unable to talk, eat properly, or take care of himself.

Son of sevenless homolog 1 (SOS1) inhibitors have been detailed in a Shanghai Allist Pharmaceuticals Co. Ltd. patent and described as useful for the treatment of cancer, arteriovenous malformations, ...

His second child, Walker, was born with cardiofaciocutaneous syndrome (CFC); which means he will function at the level of a two-year-old, for the rest of his life.

CSPC Zhongqi Pharmaceutical Technology (Shijiazhuang) Co. Ltd. has identified son of sevenless homolog 1 (SOS1)/GTPase KRAS (G12D mutant) interaction inhibitors reported to be useful for the treatment ...

His second child, Walker, was born with an extremely rare genetic disability, cardiofaciocutaneous syndrome (CFC), which means he will function at the level of a two-year-old, for the rest of his ...

KINSTON, N.C. (WITN) - A child with a rare disorder has been sworn in as Kinston’s newest police officer. When he was 4 years old, Levi Scott was diagnosed with Cardiofaciocutaneous Syndrome, a ...