Cardiofaciocutaneous (CFC) syndrome is a rare genetic disorder marked by congenital heart disease, distinctive craniofacial appearance, musculoskeletal, dermatologic, and gastrointestinal ...

When he was 8 months old, Walker Brown was diagnosed with cardiofaciocutaneous syndrome (CFC), a rare disorder that left him with severe cognitive, developmental and physical disabilities.

Myli's first few weeks were rough and it took months to get a definitive diagnosis through a blood test: CFC syndrome, cardiofaciocutaneous syndrome. It is caused by a random genetic mutation. "It ...

Michael has a rare condition called Cardio-Facio-Cutaneous (CFC) syndrome, marked by congenital heart defects, scoliosis, eye problems, learning disabilities and other problems. The family is ...

One is known as cardio-facio-cutaneous, or CFC, syndrome, for which she and her team discovered the genes responsible last year. The other two are called Noonan syndrome and Costello syndrome. In a ...

The RASopathies, which include Noonan syndrome (NS) and Cardiofaciocutaneous syndrome (CFC), are autosomal dominant disorders with genetic heterogeneity associated with germline mutations of genes ...

KRAS: More severe cognitive delay, skin and hair findings resembling cardiofaciocutaneous syndrome. SOS1: Lower prevalence of short stature and of cognitive delays, skin and hair findings ...

Hunter was diagnosed at the age of 10 with cardiofaciocutaneous syndrome, or CFC, a serious condition that can manifest in abnormal facial features, slower hair growth, heart malformation and ...

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 ...