Although cystic fibrosis is a single gene mutation, there are more than 1,000 different ways the CFTR gene can mutate in ...

The Hospital for Sick Children. "Newly uncovered mechanism could drive next-gen cystic fibrosis treatments." ScienceDaily. ScienceDaily, 13 March 2025. <www.sciencedaily.com / releases / 2025 / 03 / ...

From today, the updated indication for TRIKAFTA is as follows: TRIKAFTA is indicated for the treatment of cystic fibrosis in patients aged 2 years and older who have at least one F508del mutation in ...

Learning from examples like congenital heart disease and cystic fibrosis can help health systems and clinicians prepare to care for an influx of patients with neuromuscular diseases as they reach ...

Studying how proteins cluster and organize themselves at the cell membrane could pave the way for innovative cystic fibrosis ...

A new research project focusing on rare genetic mutations that are linked to cystic fibrosis just received $600,000 in ...

The genetic condition cystic fibrosis had no treatments on the NHS before 2019 and a Daily Express campaign - now a miracle ...

Two parents from Bexleyheath are set to take on the London Marathon to raise money for three incredible heart charities.

Rare Disease Day was observed last Friday by a group of volunteers who took an hour out of their schedule to create awareness ...

Rebecca Richards, a Montana parent of a child with disabilities, is among those worried about the implications of the cuts.

It has been six months since the N.W.T. government introduced its revamped extended health benefits (EHB) program, which ...