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Rev. bras. oftalmol ; 75(1): 61-63, jan.-fev. 2016. graf
Article in English | LILACS | ID: lil-771117

ABSTRACT

RESUMO Relato de caso de distrofia muscular oculofaríngea, doença genética de herança autossômica dominante e uma das causas de ptose miogênica adquirida. A paciente apresentou quadro de ptose palpebral bilateral e disfagia, achados clínicos típicos da doença, foi submetida a tratamento cirúrgico da ptose, com bom resultado estético e funcional.


ABSTRACT The authors report a case of oculopharyngeal muscular dystrophy, an autosomal dominant genetic disease, which leads to miogenic ptosis. This patient presented bilateral palpebral ptosis and dysphagia and underwent ptosis surgical treatment, with a good functional and aesthetic result.


Subject(s)
Humans , Female , Middle Aged , Blepharoptosis/surgery , Blepharoptosis/etiology , Ocular Motility Disorders/surgery , Ocular Motility Disorders/etiology , Blepharoplasty/methods , Muscular Dystrophy, Oculopharyngeal/complications , Blepharoptosis/diagnosis , Deglutition Disorders , Ocular Motility Disorders/diagnosis , Muscular Dystrophy, Oculopharyngeal/diagnosis , Eyelids/surgery , Eyelids/pathology , Oculomotor Muscles/surgery , Oculomotor Muscles/pathology
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