Cystinosis Foundation UK

Cystinosis Foundation UK are supporting research that will help in finding a cure and improving the medicines we have to treat cystinosis. Cystinosis is a rare inherited disease occurring in about 1 in 200,000 births within developed countries. It occurs when the mechanism removing excess cystine (an amino acid) breaks down. Cystinosis Foundation UK has multiple aims: - Provide support to all diagnosed with cystinosis, their families and relatives - Provide relevant, accessible and up to date information about the disorder - Publish newsletters containing relevant information for parents and supporters - Organise or participate in conferences relevant to cystinosis - Support research into the treatment of cystinosis

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