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利用肌酸激酶检测严重X连锁型肌营养不良症携带者。

Use of creatine kinase for detecting severe X-linked muscular dystrophy carriers.

作者信息

Dennis N R, Evans K, Clayton B, Carter C O

出版信息

Br Med J. 1976 Sep 4;2(6035):577-9. doi: 10.1136/bmj.2.6035.577.

Abstract

Women thought to be at risk of being carriers of Duchenne muscular dystrophy were given "odds" against their having an affected child. These were calcuated from a combination of the genetic risk from the family history and an estimation of the biochemical risk from measuring the serum creatine kinase concentration. The women were told the actual risk estimate and it was put into perspective for them as a high, medium, or low risk. Of 25 women at high risk six have had children, all girls; the two in the medium-risk group have had no children; and the 46 women at low risk have had 19 boys and 25 girls. None of the boys has the disease. With detailed counselling most potential carriers of this disease reach decisions in child bearing that are in line with their degree of risk.

摘要

被认为有杜氏肌营养不良症携带者风险的女性,被告知她们生育患病孩子的“几率”。这些几率是根据家族病史的遗传风险以及通过测量血清肌酸激酶浓度估算的生化风险综合计算得出的。这些女性被告知实际的风险评估结果,并从高、中、低风险的角度为她们进行了说明。在25名高风险女性中,有6人生育了孩子,都是女孩;中风险组的2名女性没有孩子;46名低风险女性生育了19名男孩和25名女孩。没有男孩患病。通过详细的咨询,这种疾病的大多数潜在携带者在生育问题上做出的决定与其风险程度相符。

相似文献

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Carrier detection and genetic counselling in Duchenne dystrophy.杜氏肌营养不良症的携带者检测与遗传咨询
Dev Med Child Neurol. 1975 Jun;17(3):352-6. doi: 10.1111/j.1469-8749.1975.tb04674.x.

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