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Abstract
Sam Berns was diagnosed with progeria, a rare genetic disease marked by premature ageing, when he was 22 months old. For the next 15 years, he and his family catalysed a multidisciplinary effort to find a cure for the disease.
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Sam Berns was diagnosed with progeria, a rare genetic disease marked by premature ageing, when he was 22 months old. For the next 15 years, he and his family catalysed a multidisciplinary effort to find a cure for the disease.