Flail arm syndrome with several issues related to the diagnostic process |
Jae-Youn Kim, Yun Kyung Park, Bora Yoon, Kee Ook Lee, Yong-Duk Kim, and Sang-Jun Na |
Department of Neurology, Konyang University of College of Medicine, Daejeon, Korea |
Corresponding Author:
Sang-Jun Na ,Tel: +82-42-600-8814, Fax: +82-42-545-0050, Email: nukedoc@hanmail.net |
Received September 2, 2016 Accepted January 2, 2017 |
Copyright © 2017 The Korean Society of Clinical Neurophysiology |
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium,
provided the original work is properly cited. |
ABSTRACT |
Flail arm syndrome (FAS), known as one of the atypical amyotrophic lateral sclerosis (ALS) variants, has a similar clinical course and pathologic findings as ALS. Therefore it is difficult to differentiate between ALS and FAS at a glance. There are few reports involving individual analysis of FAS patients to date. The findings of polysomnography (PSG) in patient with FAS are not well known. We report a male FAS patient with review of literatures and several issues related to the diagnostic process. |
Key words:
Flail arm syndrome; Amyotrophic lateral sclerosis; Upper motor neuron sign |
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