Monomelic amyotrophy with late progression

Citation
J. Rowin et al., Monomelic amyotrophy with late progression, NEUROMUSC D, 11(3), 2001, pp. 305-308
Citations number
11
Categorie Soggetti
Neurosciences & Behavoir
Journal title
NEUROMUSCULAR DISORDERS
ISSN journal
09608966 → ACNP
Volume
11
Issue
3
Year of publication
2001
Pages
305 - 308
Database
ISI
SICI code
0960-8966(200104)11:3<305:MAWLP>2.0.ZU;2-T
Abstract
Monomelic amyotrophy is a sporadic juvenile-onset disease that presents wit h gradual onset of weakness and atrophy in the hand muscles unilaterally. G enerally, this disease is considered a 'benign' and non-progressive motor n euron disease, which stabilizes within five years of onset. We discuss a ca se that illustrates that monomelic amyotrophy may rarely exhibit late clini cal progression to the lower extremities after a prolonged period of diseas e stability. (C) 2001 Elsevier Science B.V. All rights reserved.