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A Child with Acromelalgia due to Fabry’s Disease Treated with Myrogabalin Eyan TAKAYAMA 1 , Nozomi MAJIMA 1 , Hideki MATSUMURA 2 , Toshiaki MINAMI 1 1Department of Anesthesiology, Osaka Medical and Pharmaceutical University 2Department of Pediatrics, Osaka Medical and Pharmaceutical University Keyword: Fabry’s disease , acrodermal pain , pediatric , neuropathic pain pp.64-68
Published Date 2024/1/10
DOI https://doi.org/10.18916/masui.2024010013
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 Fabry’s disease is an X-linked inherited inborn error of metabolism caused by a genetic mutation of the lysosomal enzyme α-galactosidase A. We report the case details of a 14-year-old Japanese boy with Fabry’s disease whose pain was difficult to control but responded well to the gabapentinoid medication myrogabalin.


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電子版ISSN 印刷版ISSN 0021-4892 克誠堂出版

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