我们应该对斯坦纳特病进行系统性电生理研究吗？
Should we perform systematic electrophysiological study in Steinert's disease?
作者信息
Fayssoil Abdallah
出版信息
J Cardiothorac Surg. 2008 Oct 18;3:56. doi: 10.1186/1749-8090-3-56.
Abstract
Myotonic dystrophy type 1 (Steinert's disease) is a multisystem disorder with autosomal dominant inheritance. This disease is associated with the presence of an abnormal expansion of a cytosine thymine-guanine (CTG) trinucleotide repeat on chromosome 19q13.3. Because of rhythmic complications, the place for systematic electrophysiological study (EPS) has to be discussed.
摘要
1型强直性肌营养不良症（斯坦纳特病）是一种具有常染色体显性遗传的多系统疾病。该疾病与19号染色体长臂1区3带（19q13.3）上胞嘧啶-胸腺嘧啶-鸟嘌呤（CTG）三核苷酸重复序列的异常扩增有关。由于存在节律性并发症，必须讨论进行系统电生理研究（EPS）的地点。
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