What Is Cardiofaciocutaneous (CFC) Syndrome? Cardiofaciocutaneous (CFC) syndrome is a rare genetic condition. It is one in a group of conditions called RASopathies (raz-OP-uh-thees). These happen when ...

What Is Cardiofaciocutaneous (CFC) Syndrome? Cardiofaciocutaneous (CFC) syndrome is a rare genetic condition. It is one in a group of conditions called RASopathies (raz-OP-uh-thees). These happen when ...

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 ...

Cardiofaciocutaneous syndrome (CFC) is a rare genetic disorder that is believed to strike one in 810,000 people. Charities believe that the actual incidence of CFC may be much higher, because it ...

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

Background: Cardio-Facio-Cutaneous syndrome (CFCS) is a rare autosomal dominant genetic disorder primarily caused by BRAF gene mutations, posing diagnostic challenges due to its multifaceted clinical ...

8. Szczawińska-Popłonyk A, Popłonyk N, Niedziela M, Sowińska-Seidler A, Sztromwasser P, Jamsheer A, et al. Case report: The cardio-facio-cutaneous syndrome due to a novel germline mutation in MAP2K1: ...

Cardiofaciocutaneous (CFC) syndrome (MIM 115150) is a multiple congenital anomalies/mental retardation syndrome characterised by congenital heart defects, characteristic facial appearance, short ...

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.