Dysphonia as an unusual debut of parsonage-Turner syndrome

6Citations
Citations of this article
23Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Background Parsonage-Turner syndrome is a rare and painful peripheral neuropathy that usually presents as brachial plexus neuritis and also has other nerve involvement. Methods and Results Herein, we report the case of a patient with right recurrent nerve palsy as the first clinically isolated manifestation of underlying Parsonage-Turner syndrome. Idiopathic dysphonia was the only symptom presenting during a week for a patient that later developed a more conventional neurological deficit in her right shoulder. Conclusions The case illustrates the need for a careful clinical-neurologic examination beyond the larynx in patients presenting with idiopathic dysphonia. Parsonage-Turner syndrome should be considered as one of the rare causes in the differential diagnosis of isolated and otherwise unexplained dysphonia. Copyright © 2012 Wiley Periodicals, Inc.

Cite

CITATION STYLE

APA

Samarà, L., Valls-Sole, J., & Caballero, M. (2013). Dysphonia as an unusual debut of parsonage-Turner syndrome. Head and Neck, 35(7). https://doi.org/10.1002/hed.23055

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free