P67L: a cystic fibrosis allele with mild effects found at high frequency in the Scottish population.

Alec Gilfillan, Jon Warner, J M Kirk, T. Marshall, A P Greening, Ling‐Pei Ho, T. B. Hargreave, B.H.R. Stack, Dan McIntyre, R Davidson,

Journal of Medical Genetics · 1998 · 17 citations · 21 references

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Abstract

Only three mutant cystic fibrosis (CF) alleles have to date been established as conferring a dominant mild effect on affected subjects who are compound heterozygotes. We now add a fourth, P67L, which occurs on about 1.4% of Scottish CF chromosomes. Among 13 patients (12 unrelated) with this allele, the average age at diagnosis was 22.5 +/- 11.3 years. None of the cases had consistently raised sweat chloride concentrations, the average value being 57 +/- 9 mmol/l; 77% of the patients were pancreatic sufficient. When compared to three other established mild CF alleles, R117H, A455E, and 3849 + 10kb C-T, a compound heterozygote for P67L has minimal disease and clinical suspicions are unlikely to be confirmed other than by DNA typing.

References

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