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

被引:12
作者
Gilfillan, A
Warner, JP
Kirk, JM
Marshall, T
Greening, A
Ho, LP
Hargreave, T
Stack, B
McIntyre, D
Davidson, R
Dean, JCS
Middleton, W
Brock, DJH [1 ]
机构
[1] Univ Edinburgh, Western Gen Hosp, Mol Med Ctr, Human Genet Unit, Edinburgh EH4 2XU, Midlothian, Scotland
[2] Royal Hosp Sick Children, Edinburgh EH9 1LF, Midlothian, Scotland
[3] Gartnavel Gen Hosp, Glasgow G12 0YN, Lanark, Scotland
[4] Victoria Infirm, Glasgow G42 9TY, Lanark, Scotland
[5] Duncan Guthrie Inst Med Genet, Glasgow G3 8SJ, Lanark, Scotland
[6] Aberdeen Royal Hosp NHS Trust, Dept Med Genet, Aberdeen AB25 2ZD, Scotland
[7] St Johns Hosp, Med Unit, Livingston EH54 6PP, Scotland
关键词
cystic fibrosis; dominant effect; P67L;
D O I
10.1136/jmg.35.2.122
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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.
引用
收藏
页码:122 / 125
页数:4
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