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dc.contributor.authorHakyemez, Ömer Serdar
dc.contributor.authorArslanoğlu, Fatih
dc.contributor.authorBirinci, Murat
dc.contributor.authorÇaçan, Mehmet Akif
dc.contributor.authorKara, Adnan
dc.date.accessioned2020-03-05T08:01:47Z
dc.date.available2020-03-05T08:01:47Z
dc.date.issued2019en_US
dc.identifier.citationHakyemez, Ö. S., Arslanoğlu, F., Birinci, M., Çaçan, M. A. ve Kara, A. (2019). Acute carpal tunnel syndrome secondary to amyloidosis. Hindawi. https://doi.org/10.1155/2019/1610430en_US
dc.identifier.urihttp://doi.org/10.1155/2019/1610430
dc.identifier.urihttps://hdl.handle.net/20.500.12511/4995
dc.description.abstractIntroduction. ACTS secondary to amyloidosis is a very rare situation in the literature, and here, we present a unique case of ACTS secondary to amyloidosis. Case Report. A 61-year-old male patient was admitted to our hospital with complaints of numbness in the lateral half of his 1, 2, 3, and 4 fingers of his right hand. These complaints started acutely, and the patient did not have a history of trauma. His clinical examination was suitable for acute carpal tunnel syndrome. Discussion. Carpal tunnel syndrome, as well as acute carpal tunnel syndrome, may occur based on different causes. ACTS is very rare, especially when it is not caused by a trauma. Here, we presented a unique case of ACTS based on amyloidosis. Conclusion. It should be kept in mind when ACTS may occur in patients with the diagnosis of amyloidosis.en_US
dc.language.isoengen_US
dc.publisherHindawien_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectAmyloidosisen_US
dc.subjectSyndromeen_US
dc.subjectAcute Carpal Tunnelen_US
dc.titleAcute carpal tunnel syndrome secondary to amyloidosisen_US
dc.typearticleen_US
dc.relation.ispartofCase Reports in Orthopedicsen_US
dc.departmentİstanbul Medipol Üniversitesi, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümü, Ortopedi ve Travmatoloji Ana Bilim Dalıen_US
dc.authorid0000-0003-1448-2656en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.doi10.1155/2019/1610430en_US


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