Abstract
Disorders of motor neurons include amyotrophic lateral sclerosis (ALS), primary lateral sclerosis (PLS), spinobulbar muscular atrophy (SBMA, or Kennedy’s disease), spinal muscular atrophy (SMA), poliomyelitis, and monomelic amyotrophy (Hirayama disease). Although the pathology, genetics, and clinical features of ALS are well-established, neither a unifying etiology nor a highly effective treatment have been identified. Because of this, as well as its inexorable progression and numerous clinical manifestations, the management of ALS currently requires multidisciplinary care. People living with ALS, PLS and SBMA have overlapping needs and are commonly cared for in the same multidisciplinary setting. The differential diagnosis of ALS, including conditions that can mimic ALS, are discussed as well.
Original language | English (US) |
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Title of host publication | Clinical Handbook of Neuromuscular Medicine, Second Edition |
Publisher | Springer Nature |
Pages | 173-192 |
Number of pages | 20 |
ISBN (Electronic) | 9783031704598 |
ISBN (Print) | 9783031704581 |
DOIs | |
State | Published - Jan 1 2025 |
Bibliographical note
Publisher Copyright:© The Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Nature Switzerland AG 2018, 2024.