Oculopharyngeal muscular dystrophy or oculopharyngeal distal myopathy: case report.
نویسندگان
چکیده
a Universidade Federal de São Paulo (UNIFESP), Fellowship em Otorrinolaringologia Pediátrica, São Paulo, SP, Brazil b Universidade Federal de São Paulo (UNIFESP), Fellowship em Laringologia, São Paulo, SP, Brazil c Universidade Federal de São Paulo (UNIFESP), Departamento de Fonoaudiologia, São Paulo, SP, Brazil d Universidade Federal de São Paulo (UNIFESP), Departamento de ORL-CCP, São Paulo, SP, Brazil e Universidade Nove de Julho (UNINOVE), São Paulo, SP, Brazil
منابع مشابه
Autosomal recessive oculopharyngodistal myopathy: a distinct phenotypical, histological, and genetic entity.
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متن کاملAn 81-year-old man from a family with a history of oculopharyngeal mus-
cular dystrophy (OPMD) involving 6 members over 4 generations is described. The patient first noted drooping of his eyelids at the age of 65. Dysphagia and dysarthria occurred soon thereafter. At age 78, impairment of gait developed and progressive wasting occurred in the limbs with an initial distal distribution. Electromyography of several limb muscles displayed a mixed myopathic and neurogen...
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ورودعنوان ژورنال:
- Brazilian journal of otorhinolaryngology
دوره 83 2 شماره
صفحات -
تاریخ انتشار 2017