| Literature DB >> 26515619 |
Jeffrey M Statland1, Richard J Barohn2, Mazen M Dimachkie2, Mary Kay Floeter3, Hiroshi Mitsumoto4.
Abstract
Primary lateral sclerosis is characterized by insidious onset of progressive upper motor neuron dysfunction in the absence of clinical signs of lower motor neuron involvement. Patients experience stiffness; decreased balance and coordination; mild weakness; and, if the bulbar region is affected, difficulty speaking and swallowing, and emotional lability. The diagnosis is made based on clinical history, typical examination findings, and diagnostic testing negative for other causes of upper motor neuron dysfunction. Electromyogram is normal, or only shows mild neurogenic findings in a few muscles, not meeting El Escorial criteria. Treatment is largely supportive.Entities:
Keywords: Motor neuron disease; Neuroimaging; Primary lateral sclerosis; Pseudobulbar affect; Spastic quadriparesis; Upper motor neuron disease
Mesh:
Year: 2015 PMID: 26515619 PMCID: PMC4628724 DOI: 10.1016/j.ncl.2015.07.007
Source DB: PubMed Journal: Neurol Clin ISSN: 0733-8619 Impact factor: 3.806