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X-linked bulbospinal muscular atrophy (Kennedy's syndrome): a report of three cases.

作者信息

Ertekin C, Sirin H

机构信息

Department of Neurology, Medical School Hospital, Aegean University, Bornova, Izmir, Turkey.

出版信息

Acta Neurol Scand. 1993 Jan;87(1):56-61. doi: 10.1111/j.1600-0404.1993.tb04076.x.

DOI:10.1111/j.1600-0404.1993.tb04076.x
PMID:8424313
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.

摘要

相似文献

1
X-linked bulbospinal muscular atrophy (Kennedy's syndrome): a report of three cases.
Acta Neurol Scand. 1993 Jan;87(1):56-61. doi: 10.1111/j.1600-0404.1993.tb04076.x.
2
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J Neurol. 1996 May;243(5):388-92. doi: 10.1007/BF00868997.
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[X-linked bulbo-spinal neuronopathy. Kennedy's syndrome].
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Zh Nevrol Psikhiatr Im S S Korsakova. 1993;93(2):84-6.
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Ideggyogy Sz. 2002 Sep 20;55(9-10):323-9.
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[X-linked recessive bulbospinal muscular atrophy (Kennedy's disease). A family study].
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Clinical and electrodiagnostic features of X-linked recessive bulbospinal neuronopathy.X连锁隐性延髓脊髓神经元病的临床和电诊断特征
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