| Literature DB >> 24014582 |
Dolores Gonzalez-Moron1, Jose Bueri, Marcelo Andres Kauffman.
Abstract
We described a case of a patient with autosomal dominant progressive external ophthalmoplegia (PEO) who presented with the acute onset dysphagia, quadriparesis, ptosis and respiratory insufficiency following a cardiac procedure and mimicking a myasthenic crisis. A pathogenic mutation in the C10orf2 (PEO1) gene was confirmed. The unusual presentation of our patient contributes to expand the clinical phenotype of PEO1 mutations and reinforces the need to consider mitochondrial myopathy as differential diagnosis of myasthenia gravis even in the case of acute onset symptoms.Entities:
Mesh:
Substances:
Year: 2013 PMID: 24014582 PMCID: PMC3794138 DOI: 10.1136/bcr-2013-010181
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X