Clinical characteristics and interdepartmental collaboration for patients with Anderson–Fabry disease in Shiga Prefecture, Japan
The family history and genetic testing are useful for the precise diagnosis and treatment of patients with AFD. As such patients require interdisciplinary treatment, interdepartmental cooperation should be promoted for their systemic care.
Authors
- Shinji Kume (ORCID: https://orcid.org/0000-0001-6937-9715)
- Kosuke Yamahara (ORCID: https://orcid.org/0000-0001-9487-8575)
- Hiroshi Sakai (ORCID: https://orcid.org/0000-0001-7847-030X)
- Yu Mimura (ORCID: https://orcid.org/0000-0003-0538-6785)
- Koichi Kato (ORCID: https://orcid.org/0000-0002-6125-0789)
- Yoshihisa Nakagawa (ORCID: https://orcid.org/0000-0002-9411-9314)
- Shunsuke Takagi (ORCID: https://orcid.org/0000-0002-8732-6323)
- Daisuke Tomioka
- Fumiko Nakazeki
- Ayano Takagi
- Ryosuke Fukazawa
- Ueno Yoshiki
Institutions
- Toyobo (Japan) (JP)
- Shiga University of Medical Science (JP)
- Kyoto Prefectural University of Medicine (JP)
- Koga Hospital (JP)
- Otsu Red Cross Hospital (JP)
- Nagahama City Hospital (JP)
Publication Details
- Journal
- Molecular Genetics and Metabolism Reports
- Published
- 2025-05-10
- DOI
- https://doi.org/10.1016/j.ymgmr.2025.101227
- Primary Topic
- Lysosomal Storage Disorders Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00