PubMed Health⌕ Search

PubMed · 3154738

Isolated levator myositis.

Abstract

A 54-year-old woman presented with a 1-day history of ptosis of the left upper lid. On examination, the patient exhibited a moderate ptosis, poor levator function, lid lag on down-gaze, and no limitation of ocular motility. A computed tomography (CT) scan with contrast demonstrated enhancement of the levator muscle and levator aponeurosis on the involved side. Treatment consisted of systemic steroid administration and led to complete resolution of the ptosis in 2 weeks. The combined clinical and CT scan findings give a characteristic pattern of an isolated levator myositis.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

C D Rice, L D Gray. 1988. Isolated levator myositis.. https://doi.org/10.1097/00002341-198804030-00009

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

Identification of a novel mutation in a Korean patient with oculopharyngeal muscular dystrophy.

Oculopharyngeal muscular dystrophy (OPMD) is a late-onset muscle disorder characterized by progressive dysphagia and bilateral ptosis. Mutations in the polyadenylate binding protein nuclear 1 (PABPN1) gene have been found to cause OPMD. The typical mutation is a stable trinucleotide repeat expansion in the first exon of the PABPN1 gene, in which (GCG)(6) is the normal repeat length. We investigated a Korean patient with OPMD and identified a novel mutation: a heterozygous insertion of a 9-bp sequence [(GCG)(GCA)(GCA); c.27_28insGCGGCAGCA] instead of the (GCG) repeat expansion, resulting in an in-frame insertion of three alanines (p.A10insAAA). To the best of our knowledge, this is the first report of a genetically confirmed case of OPMD in Korea.

Blepharoptosis↗