| Literature DB >> 26515621 |
Omar Jawdat1, Jeffrey M Statland2, Richard J Barohn1, Jonathan S Katz3, Mazen M Dimachkie1.
Abstract
Amyotrophic lateral sclerosis (ALS), a rapidly progressive, invariably fatal disease, involves mixed upper and lower motor neurons in different spinal cord regions. Patients with bulbar onset progress more rapidly than patients with limb onset or with a lower motor neuron presentation. Recent descriptions of regional variants suggest some patients have ALS isolated to a single spinal region for many years, including brachial amyotrophic diplegia, leg amyotrophic diplegia, and isolated bulbar palsy. Clearer definitions of regional variants will have implications for prognosis, understanding the pathophysiology of ALS, identifying genetic factors related to slower disease progression, and future planning of clinical trials.Entities:
Keywords: Amyotrophic lateral sclerosis; Brachial amyotrophic diplegia; Flail arm; Flail leg; Isolated bulbar ALS; Leg amyotrophic diplegia; Motor neuron disease
Mesh:
Year: 2015 PMID: 26515621 PMCID: PMC4629514 DOI: 10.1016/j.ncl.2015.07.003
Source DB: PubMed Journal: Neurol Clin ISSN: 0733-8619 Impact factor: 3.806