Progressive Muscular Dystrophy (Erb.)
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چکیده
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 کاملDystrophy, abiotrophy, amyotrophy.
Dystrophic is the adjective pertaining to, or characterized by dystrophy. It applies to any degenerative disorder resulting from inadequate nutrition, or more specifi cally to muscular dystrophy. Amyotrophy is another closely related word, meaning literally lack of muscle growth or nourishment, but often used imprecisely or loosely to mean acquired muscle wasting, e.g. neuralgic amyotrophy, dia...
متن کاملFacioscapulohumeral Muscular Dystrophy: The Molecular Signaling Pathway
Submit Manuscript | http://medcraveonline.com Facioscapulohumeral muscular dystrophy (FSHD) is the third most common myopathy found in adults, with an overall incidence of more than 1:20000 (source: Orphanet). It is classified among progressive muscular dystrophies, characterized by muscular fiber necrosis and degeneration giving rise to progressive muscular weakness and atrophy. Weakness usual...
متن کاملEarly observations on duchenne-meryon muscular dystrophy.
cles, loss of ambulation by adolescence, and early death. His harpoon muscle biopsies established the loss of muscle fi bre striation, hyperplasia of fi brous connective tissue with replacement by granular matter and fat vesicles, and fascicular atrophy of the muscles and destruction of the muscle as essential features. Duchenne wrote [4] : ‘This disease is mainly characterised: (1) By feeblene...
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...
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