Cricopharyngeal achalasia is a common cause of dysphagia in patients with mtDNA deletions

Citation
C. Kornblum et al., Cricopharyngeal achalasia is a common cause of dysphagia in patients with mtDNA deletions, NEUROLOGY, 56(10), 2001, pp. 1409-1412
Citations number
10
Categorie Soggetti
Neurology,"Neurosciences & Behavoir
Journal title
NEUROLOGY
ISSN journal
00283878 → ACNP
Volume
56
Issue
10
Year of publication
2001
Pages
1409 - 1412
Database
ISI
SICI code
0028-3878(20010522)56:10<1409:CAIACC>2.0.ZU;2-9
Abstract
To assess dysphagia, the authors examined 12 patients with Kearns-Sayre syn drome (KSS) or chronic progressive external ophthalmoplegia (CPEO) due to m itochondrial DNA (mtDNA) deletion by videofluoroscopy and manometry. Cricop haryngeal achalasia was documented in nine of 12 patients (75%), whereas de glutitive coordination problems were found in one patient. Cricopharyngeal! myotomy may be an effective treatment in selected cases with severe cricop haryngeal obstruction.