Dysarthria and Dysphagia in Amyotrophic Lateral Sclerosis: A Case Study
Keywords:
Amyotrophic Lateral Sclerosis, Dysarthria, Dysphagia, Motor NeuronsAbstract
Amyotrophic lateral sclerosis (ALS) is the most common motor neuron disease affecting the bulbar, limb and respiratory muscles. ALS is generally characterized by progressive degeneration of both upper motor neuron (UMN) and lower motor neuron (LMN) dysfunction leading to a ‘mixed’ spastic-flaccid dysarthria. To date, only a few studies have been published regarding the nature of speech characteristics and dysphagia during the developmental course of ALS. The present study highlighted the nature of speech impairment and swallowing difficulties in a 36-year-old male who was diagnosed as having ALS with bulbar signs. Speech evaluation indicated the presence of flaccid spastic mixed dysarthria. His speech was characterized by hypernasality, imprecise consonants, distorted vowels, harshness, short phrases, mono-pitch, mono-loudness, silent pauses, prolonged phonemes, slow rate of speech, leading to poor speech intelligibility. Also, the swallowing assessment revealed a moderate degree of dysphagia because of the “bulbar onset” of ALS. Knowledge of speech, language and swallowing characteristics in individuals with ALS is crucial, as it helps the professionals and the caregivers to give a better service. This knowledge is often used for rehabilitation, employment, participation in the community, and to inform the role of family members in the betterment of the patient.
Keywords: amyotrophic lateral sclerosis (ALS), degeneration, dysarthria, dysphagia, motor neurons
Cite this Article
Theaja Kuriakose, Girish K.S. Dysarthria and Dysphagia in Amyotrophic Lateral Sclerosis: A Case Study. Research & Reviews: A Journal of Neuroscience. 2020; 10(3): 12–19p.
Downloads
Published
Issue
Section
License
Declaration and Copyright Transfer Form
(to be completed by authors)
I/ We, the undersigned author(s) of the submitted manuscript, hereby declare, that the above manuscript which is submitted for publication in the STM Journals(s), is not published already in part or whole (except in the form of abstract) in any journal or magazine for private or public circulation, and, is not under consideration of publication elsewhere.
- I/We will not withdraw the manuscript after 1 week of submission as I have read the Author Guidelines and will adhere to the guidelines.
- I/We Author(s ) have niether given nor will give this manuscript elsewhere for publishing after submitting in STM Journal(s).
- I/ We have read the original version of the manuscript and am/ are responsible for the thought contents embodied in it. The work dealt in the manuscript is my/ our own, and my/ our individual contribution to this work is significant enough to qualify for authorship.
- I/We also agree to the authorship of the article in the following order:
Author’s name
1. ________________
2. ________________
3. ________________
4. ________________
| We Author(s) tick this box and would request you to consider it as our signature as we agree to the terms of this Copyright Notice, which will apply to this submission if and when it is published by this journal. |