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Investigating the role of genetic counseling in neuromuscular disease considering life events

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Please use this identifier to cite or link to this item:http://hdl.handle.net/2115/75442

Title: Investigating the role of genetic counseling in neuromuscular disease considering life events
Authors: Shibata, Yuka Browse this author
Yabe, Ichiro Browse this author →KAKEN DB
Matsushima, Masaaki Browse this author
Hashimoto, Naoki Browse this author
Yamada, Takahiro Browse this author →KAKEN DB
Sasaki, Hidenao Browse this author →KAKEN DB
Issue Date: 13-Mar-2019
Publisher: Nature Research
Journal Title: Journal of Human Genetics
Issue: 64
Start Page: 551
End Page: 559
Publisher DOI: 10.1038/s10038-019-0590-8
Abstract: Genetic diagnoses are becoming routine in the medical practice of neuromuscular diseases. Many diagnoses, however, can have an influence on relatives and family members and thus must be handled carefully by genetic counseling (GC). Here, we aimed to assess the purpose of undergoing GC to verify the utility of collaborations between clinical and genetic divisions. We investigated consecutive GC cases of neuromuscular disease and examined the role of GC. Our study included 102 cases who underwent GC in our hospital from July 2005 to March 2018: 86.3% were women, and 45.1% were in their 30's. Disease explanation was the most common reason for attending GC (29.4%), followed by prenatal diagnosis (25.5%), pre-symptomatic diagnosis (17.6%) and carrier diagnosis (14.7%). Clients typically visited the hospital for GC when some kind of life event occurred, such as marriage, desire to bear a child, or change in condition of the proband. Clinicians should be conscious of such life events from the perspective of both the client and their relatives, and guide the GC at an appropriate time. Overall, the degree of recognition of genetic risk by clients differed, thus it is important for GC to determine the status of each unique situation and respond individually.
Rights: This is a post-peer-review, pre-copyedit version of an article published in Journal of Human Genetics. The final authenticated version is available online at: http://dx.doi.org/10.1038/s10038-019-0590-8
Type: article (author version)
URI: http://hdl.handle.net/2115/75442
Appears in Collections:医学院・医学研究院 (Graduate School of Medicine / Faculty of Medicine) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)

Submitter: 矢部 一郎

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