A Case of Autosomal Recessive Dopa Responsive Dystonia (DRD) with GCH1 Gene Mutation

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Abstract

Timely diagnosis of Segway’s disease is very important and neurologists should always consider it in the differential diagnosis of dystonia. Because the symptoms of this disease can be resolved with low doses of Levodopa and the patient can lead a normal life in the community. Another important issue is genetic counselling for these patients before marriage or pregnancy, the mode of inheritance and the risk of their children should be investigated and estimated. Here we present a case of Segawa patient who was challenging in genetic counselling.
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常染色体隐性多巴反应性肌张力障碍伴GCH1基因突变1例
及时诊断赛格威病是非常重要的,神经学家在肌张力障碍的鉴别诊断中应始终考虑到这一点。因为这种疾病的症状可以通过低剂量的左旋多巴得到解决,患者可以在社区中过正常的生活。另一个重要的问题是对这些患者在结婚或怀孕前进行遗传咨询,应调查和估计遗传方式及其子女的风险。在这里,我们提出了一例Segawa病人谁是遗传咨询挑战。
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