Author/Authors :
Asadollahi، Marjan نويسنده Assistant Professor, Department of Neurology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran , , Rezaiyan، Bibiseyedeh نويسنده Loghman Hospital, Department of Neurology, Shahid Beheshti University of Medical Sciences, Tehran, Iran. Rezaiyan, Bibiseyedeh , Amjadi، Hiva نويسنده Loghman Hospital, Department of Neurology, Shahid Beheshti University of Medical Sciences, Tehran, Iran. Amjadi, Hiva
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.
