A £1.65 million treatment has been approved for use for some NHS patients, offering hope of a cure to those with an inherited blood disorder.
Campaigners have shared their joy as health officials approved a gene-editing therapy for certain children and adults with severe sickle cell disorder.
It is estimated that 1,700 people could be eligible after the National Institute for Health and Care Excellence (Nice) approved Casgevy for certain patients with the genetic condition.
NHS officials estimate that around 50 people a year will receive treatment. Casgevy, also known as exa-cel, was the first treatment to be licensed using gene-editing tool Crispr, which earned its inventors the Nobel Prize for chemistry in 2020.
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