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Cystic fibrosis (CF) is a progressive, hereditary, autosomal recessive disorder that is more common among Caucasians. It was first described by Dorothy H. Andersen in 1938 as “cystic fibrosis of the pancreas” to classify exocrine pancreatic destruction. In 1953, Di Sant’Agnese demonstrated that these patients lose excessive salt in their sweat, leading to adoption of electrolytic methods for diagnosis of the disease.
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