Your browser doesn't support javascript.
loading
[Slowly progressive dysarthria in primary lateral sclerosis]. / Langsam progressive Dysarthrophonie bei primärer Lateralsklerose.
Urban, P P; Wellach, I; Pohlmann, C.
Affiliation
  • Urban PP; Abteilung für Neurologie, Asklepios Klinik Barmbek, Rübenkamp 220, 22291, Hamburg, Deutschland. p.urban@asklepios.com
Nervenarzt ; 81(8): 986-8, 990-1, 2010 Aug.
Article in De | MEDLINE | ID: mdl-20532474
ABSTRACT
Slowly progressive dysarthria over many years may be the only sign of primary lateral sclerosis (PLS). Clinically it presents as pseudobulbar palsy which can be differentiated from amyotrophic lateral sclerosis (ALS) by the longer disease duration (> or =4 years), central pathological magnetic-evoked potentials to the tongue and lack of denervation in EMG. In contrast, hereditary spastic paraplegia (HSP) is characterized by a primary spasticity of the lower limbs, mostly later onset, the fact that other family members are affected and in isolated cases by positive genetic testing for mutations.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Motor Neuron Disease / Pseudobulbar Palsy Type of study: Diagnostic_studies / Prognostic_studies Limits: Aged / Aged80 / Female / Humans Language: De Journal: Nervenarzt Year: 2010 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Motor Neuron Disease / Pseudobulbar Palsy Type of study: Diagnostic_studies / Prognostic_studies Limits: Aged / Aged80 / Female / Humans Language: De Journal: Nervenarzt Year: 2010 Document type: Article