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- W2201445849 abstract "While our understanding of cystic fibrosis genetics has expanded in recent decades, the genetics and clinical manifestations of the disease remains highly heterogeneous. Diagnosis of CF in non-classical mutations remains a clinical challenge. We describe the clinical presentation of two patients with chronic cough found to have normal sweat chlorides. We discuss the subsequent evaluation that lead to the diagnosis of two rare CF mutations. We briefly discuss the use of the expanded 106-panel of CF mutations (homozygous 3849 + 10 kb C > T), and the role of whole CFTR gene sequencing (heterozygous c.2752-26 A > G/5T)." @default.
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- W2201445849 date "2016-01-01" @default.
- W2201445849 modified "2023-10-16" @default.
- W2201445849 title "Chronic cough with normal sweat chloride: Phenotypic descriptions of two rare cystic fibrosis genotypes" @default.
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- W2201445849 doi "https://doi.org/10.1016/j.rmcr.2015.12.003" @default.
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