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Hirayama disease: An unusual case report

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dc.contributor.author Calisgan, Elisa
dc.contributor.author Canbay, Ali
dc.contributor.author Talu, Burcu
dc.contributor.author Tecellioglu, Mehmet
dc.contributor.author Sevimli, Reşit
dc.date.accessioned 2022-02-22T15:14:02Z
dc.date.available 2022-02-22T15:14:02Z
dc.date.issued 2018
dc.identifier.citation Calisgan, E., Canbay, A., Talu, B., Tecellioglu, M., & Sevimli, R. (2021). Hirayama disease: An unusual case report . Annals of Medical Research, en_US
dc.identifier.uri http://hdl.handle.net/11616/53880
dc.description.abstract Hirayama disease is an uncommon and rarely seen lower motor neuron disease. It is usually seen during periods of rapid growth (15-25 years). Distal upper extremities characteristically show weakness and atrophy. In this paper a case is presented of this rare, and difficult to diagnose disease, not previously reported in this age group, and the findings are discussed in the light of information of earlier cases in Turkey. A 53-year old male patient presented at Inonu University Neurology Polyclinic with complaints of motion tremor and atrophy in the left arm, which had been ongoing for 4 years. After electromyography, the deltoid, biceps, triceps, extensor digitorum communis, abductor pollicis brevis and abduction digiti minimi muscles were identified in the upper left limb. This case report presents information about the differential diagnosis, detailed symptoms and treatment methods of a Hirayama patient applying for physical therapy. en_US
dc.language.iso eng en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.title Hirayama disease: An unusual case report en_US
dc.type article en_US
dc.relation.journal Annals of Medical Research en_US
dc.contributor.department İnönü Üniversitesi en_US


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