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Sporadic Myotonic Dystrophy Type 2 in a Japanese Patient

We herein report a Japanese patient with myotonic dystrophy type 2 (DM2), which is rare in Japan. A 64-year-oldman had proximal muscle weakness and grip myotonia. Electromyography showed myotonic discharges, but dystrophia-myotonica protein kinase (DMPK) was negative for CTG repeats. A muscle biopsy...

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Detalles Bibliográficos
Autores principales:	Miyashita, Koichi, Ii, Yuichiro, Matsuyama, Hirofumi, Niwa, Atsushi, Kawana, Yosuke, Shibata, Soshi, Minami, Narihiro, Nishino, Ichizo, Tomimoto, Hidekazu
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	The Japanese Society of Internal Medicine 2023
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10641181/ https://www.ncbi.nlm.nih.gov/pubmed/36792202 http://dx.doi.org/10.2169/internalmedicine.0425-22

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