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P67L: a cystic fibrosis allele with mild effects found at high frequency in the Scottish population.
Gilfillan, A; Warner, J P; Kirk, J M; Marshall, T; Greening, A; Ho, L P; Hargreave, T; Stack, B; McIntyre, D; Davidson, R; Dean, J C; Middleton, W; Brock, D J.
Affiliation
  • Gilfillan A; Human Genetics Unit, University of Edinburgh, Western General Hospital, UK.
J Med Genet ; 35(2): 122-5, 1998 Feb.
Article in En | MEDLINE | ID: mdl-9507391
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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cystic Fibrosis / Alleles / Gene Frequency / Genetics, Population Type of study: Diagnostic_studies Limits: Adolescent / Adult / Child / Female / Humans / Infant / Male Country/Region as subject: Europa Language: En Journal: J Med Genet Year: 1998 Document type: Article Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cystic Fibrosis / Alleles / Gene Frequency / Genetics, Population Type of study: Diagnostic_studies Limits: Adolescent / Adult / Child / Female / Humans / Infant / Male Country/Region as subject: Europa Language: En Journal: J Med Genet Year: 1998 Document type: Article Country of publication: United kingdom