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Updated: Jul 15, 2026

Utility of Dissociated Intrinsic Hand Muscle Atrophy in the Diagnosis of Amyotrophic Lateral Sclerosis
Published on: March 4, 2014
The neuralgic amyotrophy consultation
1Neurologist, clinical neurophysiologist, Neuromuscular Centre Nijmegen, Dept. of Neurology and Clinical Neurophysiology, c/o 920 KNF, Radboud University Nijmegen, Medical Centre, PO Box 9101, 6500 HB, Nijmegen, The Netherlands. n.vanalfen@neuro.umcn.nl
Abstract:
Neuralgic amyotrophy is a distinct clinical syndrome with acute severe pain and patchy paresis in the shoulder and arm region. The clinical phenotype was recently found to be more comprehensive and the long-term prognosis less optimistic than usually assumed for many patients. The disorder can be idiopathic or hereditary in an autosomal dominant fashion, with only few phenotypical variations between the two. This article provides a practical overview of current knowledge on the clinical presentation, diagnosis, pathogenesis and the treatment of pain and complications.
