مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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Information Journal Paper

Title

CASE REPORT: A RARE CASE OF FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY AND MYASTHENIA GRAVIS

Pages

  28-29

Abstract

 Facioscapulohumeral muscular dystrophy (FSHD) is a common inherited muscular dystrophy presented clinically with slowly progressive weakness and wasting of facial and limb muscles and rare bulbar muscle involvement. We present herein a 70-year-old man who was a known case of FSHD with complaint of 15-day history of progressive difficulty in chewing and dysarthria and was found to have MYASTHENIA GRAVIS. Related literatures have been also reviewed.

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  • Cite

    APA: Copy

    ASADOLLAHI, MARJAN, REZAIYAN, BIBISEYEDEH, & AMJADI, HIVA. (2012). CASE REPORT: A RARE CASE OF FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY AND MYASTHENIA GRAVIS. CURRENT JOURNAL OF NEUROLOGY (IRANIAN JOURNAL OF NEUROLOGY), 11(1), 28-29. SID. https://sid.ir/paper/605650/en

    Vancouver: Copy

    ASADOLLAHI MARJAN, REZAIYAN BIBISEYEDEH, AMJADI HIVA. CASE REPORT: A RARE CASE OF FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY AND MYASTHENIA GRAVIS. CURRENT JOURNAL OF NEUROLOGY (IRANIAN JOURNAL OF NEUROLOGY)[Internet]. 2012;11(1):28-29. Available from: https://sid.ir/paper/605650/en

    IEEE: Copy

    MARJAN ASADOLLAHI, BIBISEYEDEH REZAIYAN, and HIVA AMJADI, “CASE REPORT: A RARE CASE OF FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY AND MYASTHENIA GRAVIS,” CURRENT JOURNAL OF NEUROLOGY (IRANIAN JOURNAL OF NEUROLOGY), vol. 11, no. 1, pp. 28–29, 2012, [Online]. Available: https://sid.ir/paper/605650/en

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