CARRIER DETECTION IN DUCHENNE MUSCULAR-DYSTROPHY - EVIDENCE FROM A STUDY OF OBLIGATORY CARRIERS AND MOTHERS OF ISOLATED CASES

被引:43
作者
SIBERT, JR
HARPER, PS
THOMPSON, RJ
NEWCOMBE, RG
机构
[1] UNIV WALES WELSH NATL SCH MED,DEPT CHILD HLTH,CARDIFF CF4 4XN,S GLAMORGAN,WALES
[2] UNIV WALES WELSH NATL SCH MED,DEPT MED GENET,CARDIFF CF4 4XN,S GLAMORGAN,WALES
[3] UNIV WALES WELSH NATL SCH MED,DEPT MED BIOCHEM,CARDIFF CF4 4XN,S GLAMORGAN,WALES
[4] UNIV WALES WELSH NATL SCH MED,DEPT MED STAT,CARDIFF CF4 4XN,S GLAMORGAN,WALES
[5] UNIV HOSP WALES,CARDIFF CF4 4XN,S GLAMORGAN,WALES
关键词
D O I
10.1136/adc.54.7.534
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
The mean levels of serum creatinine phosphokinase (CPK) were studied in three groups of women: normal controls (57), obligate carriers for Duchenne muscular dystrophy (30), and mothers of isolated cases of this disease (35). The distribution of the levels in these groups was significantly different and was in keeping with the hypothesis that one-third of isolated cases result from new mutations. The control and carrier ranges overlapped considerably, with the level of CPK of 33% of obligate carriers coming within the 97 1/2 centile of the normal range. Odds against an individual being a carrier were derived for specific mean values of CPK. They should be considered with genetic information using Bayes' theorem. The mean CPK levels in obligate carriers showed significant familial clustering. This may have implications in carrier detection.
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页码:534 / 537
页数:4
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