X-linked bulbospinal muscular atrophy (Kennedy's syndrome): a report of three cases
- 29 January 2009
- journal article
- case report
- Published by Hindawi Limited in Acta Neurologica Scandinavica
- Vol. 87 (1) , 56-61
- https://doi.org/10.1111/j.1600-0404.1993.tb04076.x
Abstract
Two cases of X-linked bulbo-spinal muscular atrophy and one sporadic case with the same clinical features are presented. All three cases were extensively studied by electrophysiological methods. One of the patients showed some transient weakness, which was partly improved by pyridostigmin. In this patient the Decrement test and jitter revealed a mild degree of motor-end plate dysfunction. Clinical and electrophysiological findings obtained from all three patients suggest that in Kennedy syndrome cell bodies of group IA muscle afferents are also affected selectively, with other peripheral afferents.Keywords
This publication has 23 references indexed in Scilit:
- X-linked bulbo-spinal neuronopathy of late onsetActa Neurologica Scandinavica, 2009
- X-Linked Spinal Muscular Atrophy (Kennedy's Syndrome)Archives of Neurology, 1990
- RR Interval Variation and the Sympathetic Skin Response in the Assessment of Autonomic Function in Peripheral NeuropathyArchives of Neurology, 1990
- X-LINKED RECESSIVE BULBOSPINAL NEURONOPATHYBrain, 1989
- Kennedy Disease in an Italian KindredEuropean Neurology, 1986
- X-linked recessive bulbospinal neuronopathy: a report of ten cases.Journal of Neurology, Neurosurgery & Psychiatry, 1982
- Motor neuron diseaseNeurology, 1981
- Progressive proximal spinal and bulbar muscular atrophy of late onsetNeurology, 1968
- Myasthenic syndrome in patients with amyotrophic lateral sclerosisNeurology, 1959
- FIBRILLATION AND FASCICULATION IN VOLUNTARY MUSCLEBrain, 1938