| Literature DB >> 25766368 |
Emma Foster1, Benjamin K-T Tsang2, Anthony Kam3, Elsdon Storey2, Bruce Day4, Aron Hill2.
Abstract
This article discusses three patients with likely Hirayama disease. They have no other significant past medical history and no personal or family history of other neurological disorders. Hirayama disease is a form of cervical myelopathy attributed to forward displacement of the posterior cervical dural sac on neck flexion with resultant cord compression and/or venous congestion. It is characterized by a pure motor focal amyotrophy in the distribution of C7, C8 and T1 spinal segmental-innervated muscles and differs from other motor neuron diseases by virtue of its ultimately non-progressive course.Entities:
Keywords: Cervical myelopathy; Hirayama disease; Motor focal amyotrophy; Motor neuron disease
Mesh:
Year: 2015 PMID: 25766368 DOI: 10.1016/j.jocn.2014.11.025
Source DB: PubMed Journal: J Clin Neurosci ISSN: 0967-5868 Impact factor: 1.961