a rare case of facioscapulohumeral muscular dystrophy and myasthenia gravis.

نویسندگان

marjan asadollahi loghman hospital, department of neurology, shahid beheshti university of medical sciences, tehran, iran.

bibiseyedeh rezaiyan loghman hospital, department of neurology, shahid beheshti university of medical sciences, tehran, iran.

hiva amjadi loghman hospital, department of neurology, shahid beheshti university of medical sciences, tehran, iran.

چکیده

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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A rare case of facioscapulohumeral muscular dystrophy and myasthenia gravis

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 myastheni...

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عنوان ژورنال:
iranian journal of neurology

جلد ۱۱، شماره ۱، صفحات ۲۸-۲۹

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