Document Detail


Clinical patterns in progressive muscular atrophy (PMA): a prospective study.
MedLine Citation:
PMID:  17852011     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Progressive muscular atrophy (PMA) is a form of motor neuron disease, but its outcome is not well defined, and the aim was to study the pattern of clinical progression in PMA. We studied 10 patients prospectively for 12 months. None showed clinical signs of upper motor neuron involvement at presentation or during follow-up, and all had normal transcranial magnetic stimulation studies. Four had upper limb onset, four lower limb onset and two axial onset. We used neurophysiological and strength measurements and a clinical rating scale (ALS-FRS). Seven other patients presenting with a PMA syndrome developed upper motor neuron signs during a one-year period of observation and were excluded from the study. The rate of progression was variable. At six months, only motor unit number estimation (MUNE) and ALS-FRS had decreased significantly. The Neurophysiological Index (NI) and M-wave amplitude measurements decreased at 12 months. Two patients with axial-onset disease progressed rapidly to respiratory failure. Overall the pattern of change resembled that of ALS, although some patients progressed very slowly. Axial onset, however, predicts the early onset of respiratory failure, and a poor prognosis.
Authors:
Mamede de Carvalho; Manuel Scotto; Michael Swash
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases     Volume:  8     ISSN:  1748-2968     ISO Abbreviation:  Amyotroph Lateral Scler     Publication Date:  2007 Oct 
Date Detail:
Created Date:  2007-11-06     Completed Date:  2008-01-09     Revised Date:  2009-11-17    
Medline Journal Info:
Nlm Unique ID:  101283386     Medline TA:  Amyotroph Lateral Scler     Country:  England    
Other Details:
Languages:  eng     Pagination:  296-9     Citation Subset:  IM    
Affiliation:
Department of Neurology, Hospital de Santa Maria, Neuromuscular Unit of Institute of Molecular Medicine, Faculty of Medicine in Lisbon, Portugal
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MeSH Terms
Descriptor/Qualifier:
Adult
Aged
Disease Progression
Follow-Up Studies
Humans
Male
Middle Aged
Motor Neurons / physiology*
Muscular Atrophy, Spinal / physiopathology*
Neurologic Examination
Prospective Studies
Severity of Illness Index
Statistics, Nonparametric

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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