Ptose miogênica na distrofia muscular oculofaríngea / Miogenic ptosis in oculopharyngeal muscular dystrophy
Rev. bras. oftalmol
;
75(1): 61-63, jan.-fev. 2016. graf
Article
in English
| LILACS
| ID: lil-771117
RESUMO
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
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.
Full text:
Available
Index:
LILACS (Americas)
Main subject:
Blepharoptosis
/
Ocular Motility Disorders
/
Blepharoplasty
/
Muscular Dystrophy, Oculopharyngeal
Type of study:
Diagnostic study
Limits:
Female
/
Humans
Language:
English
Journal:
Rev. bras. oftalmol
Journal subject:
Ophthalmology
Year:
2016
Type:
Article
Affiliation country:
Brazil
Institution/Affiliation country:
Hospital Universitário Bettina Ferro de Souza/BR
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