Clinical and electrophysiological characteristics of neuropathy associated with Tangier disease
Clinical and electrophysiological characteristics of neuropathy associated with Tangier disease
About this item
Full title
Author / Creator
Publisher
Berlin/Heidelberg: Springer-Verlag
Journal title
Language
English
Formats
Publication information
Publisher
Berlin/Heidelberg: Springer-Verlag
Subjects
More information
Scope and Contents
Contents
Tangier disease (TD) (OMIM#205400) is a rare autosomal recessive disorder resulting from mutations in the
ABCA1
gene, leading to decreased levels of plasma high-density lipoproteins (HDL). Peripheral neuropathy is a common finding in this disease, and may present as relapsing/remitting mono/polyneuropathies or as syringomyelia-like neuropathy...
Alternative Titles
Full title
Clinical and electrophysiological characteristics of neuropathy associated with Tangier disease
Authors, Artists and Contributors
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Primary Identifiers
Record Identifier
TN_cdi_proquest_miscellaneous_1020846295
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1020846295
Other Identifiers
ISSN
0340-5354
E-ISSN
1432-1459
DOI
10.1007/s00415-011-6340-2
