Survey on genetic counseling and health management for symptomatic and asymptomatic female dystrophinopathy carriers in Japan today

Michio Kobayashi*, Masatoshi Ishizaki, Katsuhito Adachi, Naohiro Yonemoto, Tsuyoshi Matsumura, Itaru Toyoshima, En Kimura

*この論文の責任著者

研究成果: ジャーナルへの寄稿総説査読

2 被引用数 (Scopus)

抄録

To clarify the current status of genetic counseling and health monitoring for symptomatic and asymptomatic female carriers of dystrophinopathy (Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD)), we sent out questionnaires to 104 member institutions of The Japan's National Liaison Council for Clinical Sections of Medical Genetics, and responses were received from 51 institutions. Between April 2013 and March 2014, 57 carriers at 21 institutions received genetic counseling, and 37 carriers at 15 institutions underwent genetic screening for DMD/BMD mutations. At the 23 institutions that gave genetic counseling, 20 (87%) informed carriers of possible health problems, 14 (61%) informed carriers of cardiomyopathy and heart failure, and 14 (61%) advised carriers about regular medical checkups. Evidence based on accurate and up-to-date epidemiological studies of female carriers is needed and should be widely shared with the families, medical providers, and society.

本文言語英語
ページ(範囲)407-412
ページ数6
ジャーナルClinical Neurology
56
6
DOI
出版ステータス出版済み - 2016

ASJC Scopus 主題領域

  • 臨床神経学

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