منابع مشابه
Association of Limb-Girdle muscular dystrophy with multiple sclerosis: A case report
Background: The association of limb-girdle muscular dystrophy (LGMD) with other neurological disorders is uncommon. Case presentation: We report a 25-year-old female with LGMD who suffered from slowly progressive proximal muscular weakness and atrophy since she was 12 years of age. The patient recently presented with acute loss of left side visual acuity. After evaluation, findings were sugges...
متن کاملa 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...
متن کاملA Classical Case of Duchenne Muscular Dystrophy
An 8 year old boy was presented for difficulty in walking and muscle weakness with difficulty in climbing stairs, running and particularly in vigorous physical activities, he also had decreased strength and endurance. His parents did not have consanguineous marriage, one brother and two sisters were all healthy; no other family members were similarly affected.
متن کاملA Case of Progressive Muscular Dystrophy
(1) The method of attaining the erect position, similating the climbing method of the Aran Duchenne type. (2) No wasting of the muscles of the hands. Hypertrophy of the biceps in places. (3) The talipes position of the feet, (clawfoot). (4) The position of the back. (Myopathic lordosis). G. M., age 23. Unmarried. Kalat State. Family History.?Father alive, healthy. Mother died after one month's ...
متن کاملA case of fascioscapulohumeral muscular dystrophy misdiagnosed as Becker's muscular dystrophy for 20 years.
A 60-year-old man diagnosed clinically with Becker's muscular dystrophy 20 years ago by another physician presented with gradually progressive proximal muscle weakness since teenage years. Family history revealed a strong paternal familial inheritance pattern of similar distribution of weakness-face, forearm flexion, knee extension and foot dorsiflexion. Work-ups revealed B12 deficiency and all...
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ژورنال
عنوان ژورنال: Proceedings of the Royal Society of Medicine
سال: 1909
ISSN: 0035-9157
DOI: 10.1177/003591570900200724