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杜氏肌营养不良症携带者的心电图异常

Electrocardiographic abnormalities in carriers of Duchenne muscular dystrophy.

作者信息

Lane R J, Gardner-Medwin D, Roses A D

出版信息

Neurology. 1980 May;30(5):497-501. doi: 10.1212/wnl.30.5.497.

DOI:10.1212/wnl.30.5.497
PMID:7189255
Abstract

Electrocardiographic (ECG) abnormalities characteristic of Duchenne muscular dystrophy (tall R waves in the right precordial leads and deep Q waves in the lateral chest leads) are rarely observed in carriers, but Emery (1969) found that the (R-S) amplitude sum in lead V1 was significantly greater in carriers than in age-matched controls. In a prospective single-blind study, we analyzed coded records from 11 carriers and 12 age-matched normal women for (R-S) amplitude sums and R/S ratios in leads V1 and V2. Values in carriers were significantly greater for all these characteristics, discrimination being most marked for R/S in V2 (p less than 0.01). This was confirmed in a further retrospective study, comparing records from 18 carriers with 100 normal ECGs from women of the same age range. Density functions for (R-S) in V1 and the R/S ratio in V2 derived from carrier and normal population can be incorporated into probability calculations to determine risk of carrier status.

摘要

杜氏肌营养不良的心电图(ECG)异常特征(右胸前导联R波高尖,外侧胸导联Q波深)在携带者中很少见,但埃默里(1969年)发现,携带者V1导联的(R-S)振幅总和显著高于年龄匹配的对照组。在一项前瞻性单盲研究中,我们分析了11名携带者和12名年龄匹配的正常女性的编码记录,以获取V1和V2导联的(R-S)振幅总和及R/S比值。携带者的所有这些特征值均显著更高,V2导联的R/S差异最为明显(p<0.01)。在另一项回顾性研究中得到了证实,该研究比较了18名携带者的记录与同年龄范围女性的100份正常心电图。来自携带者和正常人群的V1导联(R-S)及V2导联R/S比值的密度函数可纳入概率计算,以确定携带者状态的风险。

相似文献

1
Electrocardiographic abnormalities in carriers of Duchenne muscular dystrophy.杜氏肌营养不良症携带者的心电图异常
Neurology. 1980 May;30(5):497-501. doi: 10.1212/wnl.30.5.497.
2
An evaluation of some carrier detection techniques in Duchenne muscular dystrophy.杜氏肌营养不良症某些携带者检测技术的评估
J Neurol Sci. 1979 Nov;43(3):377-94. doi: 10.1016/0022-510x(79)90017-0.
3
Carrier detection in Duchenne muscular dystrophy: Assessment of the effect of age on detection-rate with serum-creatine-kinase-activity.杜氏肌营养不良症的携带者检测:评估年龄对血清肌酸激酶活性检测率的影响。
Lancet. 1979 Mar 31;1(8118):692-4. doi: 10.1016/s0140-6736(79)91147-4.
4
Effect of exercise on serum creatine kinase in carriers of Duchenne muscular dystrophy.运动对杜氏肌营养不良症携带者血清肌酸激酶的影响。
J Med Genet. 1982 Feb;19(1):4-7. doi: 10.1136/jmg.19.1.4.
5
Activity of creatine kinase in sera from healthy women, carriers of Duchenne muscular dystrophy and cord blood, determined by the "European" recommended method with NAC-EDTA activation.采用NAC-EDTA激活的“欧洲”推荐方法测定健康女性、杜氏肌营养不良症携带者血清及脐带血中肌酸激酶的活性。
Clin Chim Acta. 1981 Oct 26;116(2):209-16. doi: 10.1016/0009-8981(81)90024-3.
6
Serum creatine kinase activity and carrier status for duchenne muscular dystrophy.血清肌酸激酶活性与杜氏肌营养不良症的携带者状态
Lancet. 1979;2(8156-8157):1370. doi: 10.1016/s0140-6736(79)92854-x.
7
[Electro-vectorcardiographic study in Duchenne de Boulogne progressive muscular dystrophy].[进行性肌营养不良症的心电图向量图研究]
Arch Mal Coeur Vaiss. 1982 Nov;75(11):1297-309.
8
Carrier detection in Duchenne muscular dystrophy. Evidence from a study of obligatory carriers and mothers of isolated cases.杜氏肌营养不良症的携带者检测。来自对孤立病例的 obligatory 携带者和母亲的研究证据。 (注:“obligatory carriers”不太明确准确中文表述,可根据具体医学背景进一步优化)
Arch Dis Child. 1979 Jul;54(7):534-7. doi: 10.1136/adc.54.7.534.
9
Myoglobinemia in Duchenne muscular dystrophy carriers.杜氏肌营养不良症携带者的肌红蛋白血症
Brain Dev. 1980;2(1):87-8. doi: 10.1016/s0387-7604(80)80012-x.
10
Creatine kinase activity in the detection of carriers of Duchenne muscular dystrophy: comparison of two methods.肌酸激酶活性在杜氏肌营养不良症携带者检测中的应用:两种方法的比较
Clin Chim Acta. 1982 Jun 3;121(3):345-59. doi: 10.1016/0009-8981(82)90244-3.

引用本文的文献

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Interventions for preventing and treating cardiac complications in Duchenne and Becker muscular dystrophy and X-linked dilated cardiomyopathy.杜氏和贝克型肌营养不良症以及X连锁扩张型心肌病中心脏并发症的预防和治疗干预措施。
Cochrane Database Syst Rev. 2018 Oct 16;10(10):CD009068. doi: 10.1002/14651858.CD009068.pub3.
2
Cardiovascular Complications of Neuromuscular Disorders.神经肌肉疾病的心血管并发症
Curr Treat Options Cardiovasc Med. 2002 Apr;4(2):171-179. doi: 10.1007/s11936-002-0037-x.
3
Detection of mutations in the dystrophin gene via automated DHPLC screening and direct sequencing.
通过自动变性高效液相色谱筛选和直接测序检测肌营养不良蛋白基因中的突变。
BMC Genet. 2001;2:17. doi: 10.1186/1471-2156-2-17. Epub 2001 Oct 17.
4
The genetic status of mothers of isolated cases of Duchenne muscular dystrophy.杜氏肌营养不良孤立病例母亲的基因状况。
J Med Genet. 1983 Feb;20(1):1-11. doi: 10.1136/jmg.20.1.1.
5
The female carrier of Duchenne muscular dystrophy.杜氏肌营养不良症的女性携带者。
Br Med J (Clin Res Ed). 1982 May 15;284(6327):1423-4. doi: 10.1136/bmj.284.6327.1423.
6
Duchenne muscular dystrophy: pathogenetic aspects and genetic prevention.杜氏肌营养不良症:发病机制及基因预防
Hum Genet. 1984;66(1):17-40. doi: 10.1007/BF00275183.