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HERO ID
2732981
Reference Type
Journal Article
Title
Spinal and bulbar muscular atrophy: pathogenesis and clinical management
Author(s)
Grunseich, C; Rinaldi, C; Fischbeck, KH
Year
2014
Is Peer Reviewed?
1
Journal
Oral Diseases
ISSN:
1354-523X
EISSN:
1601-0825
Volume
20
Issue
1
Page Numbers
6-9
Language
English
PMID
23656576
DOI
10.1111/odi.12121
Web of Science Id
WOS:000327959500002
Abstract
Spinal and bulbar muscular atrophy, or Kennedy's disease, is an X-linked motor neuron disease caused by polyglutamine repeat expansion in the androgen receptor. The disease is characterised by weakness, atrophy and fasciculations in the limb and bulbar muscles. Affected males may have signs of androgen insensitivity, such as gynaecomastia and reduced fertility. Neurophysiological studies are typically consistent with diffuse denervation atrophy, and serum creatine kinase is usually elevated 2-5 times above normal. Progression of the disease is slow, and the focus of spinal and bulbar muscular atrophy (SBMA) management is to prevent complications.
Keywords
genetics; craniofacial; motor neuron disease; spinal and bulbar muscular atrophy; Kennedy's disease; weakness
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