[日本成人发病遗传性神经肌肉疾病症状前基因检测指南]。

Q4 Medicine
Clinical Neurology Pub Date : 2025-02-21 Epub Date: 2025-01-24 DOI:10.5692/clinicalneurol.cn-002049
Yuka Shibata, Hyangri Chang, Katsuya Nakamura, Shinichiro Yamada, Masaaki Matsushima, Kazumasa Saigoh, Hiroyuki Ishiura, Yoshiki Sekijima, Hirofumi Maruyama, Takeshi Ikeuchi, Kazuko Hasegawa, Masashi Aoki, Masahisa Katsuno, Tatsushi Toda, Ichiro Yabe
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引用次数: 0

摘要

在日本,没有针对遗传性神经肌肉疾病的症状前检测的全国性指导方针。虽然到目前为止,各机构都在使用自己的程序来处理这种情况,但有必要以日本医疗体系为基础,制定标准化的指导方针。因为疾病改善疗法的发展已经取得了进展,我们正在进入早期诊断和早期治疗的时代。本指南由日本神经学会医学遗传学委员会制定。在开发过程中,在日本各地具有丰富症状前检测经验的个人中进行了德尔菲调查,共有42名专家参与了所有三次调查,并进行了共识建立过程。最后,该指南包括45项建议,建议对成人发病的遗传性神经和肌肉疾病进行症状前检测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Guidelines for presymptomatic genetic testing for adult-onset hereditary neuromuscular diseases in Japan].

In Japan, there are no nationwide guidelines for presymptomatic testing for hereditary neuromuscular diseases. Although each institution has been dealing with this situation by using their own procedures to date, it is necessary to develop a standardized guidelines based on the Japanese medical system, because the development of disease-modifying therapies has progressed, and we are entering an era in which early diagnosis and early treatment are necessary. The guidelines presented here were devised by the Committee on Medical Genetics of the Japan Neurological Society. During their development, Delphi surveys were conducted among individuals with extensive experience in presymptomatic testing throughout Japan, with 42 experts participating in all three surveys, and a consensus-building process was undertaken. Finally, the guidelines consist of 45 recommendations for performing presymptomatic testing for adult-onset inherited neurological and muscular diseases.

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来源期刊
Clinical Neurology
Clinical Neurology Medicine-Neurology (clinical)
CiteScore
0.30
自引率
0.00%
发文量
147
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