Myopathies
Identifieur interne : 001851 ( Istex/Corpus ); précédent : 001850; suivant : 001852Myopathies
Auteurs : David Hilton-JonesSource :
- Reviews in Clinical Gerontology [ 0959-2598 ] ; 2001-05.
Abstract
Myopathy is a convenient shorthand term meaning muscle disease or dysfunction. In other words, the myopathies are those conditions in which the patient’s symptoms and signs can be attributed to a pathological process affecting either the structure of muscle fibres or their associated interstitial tissues, or to disturbance of the biochemical or electrophysiological function of those fibres. Myopathies are rare in all age ranges. They may be inherited or acquired. Onset of inherited myopathies in the elderly, not surprisingly, is uncommon, but some of these diseases are asymptomatic or cause such minor symptoms that their significance is not appreciated by the patient, and thus they may not be recognized until late on in life. Their recognition may have implications for other, younger, family members. Many of the acquired myopathies afflicting the elderly are treatable, but the commonest, inclusion body myositis, is not, and incorrect diagnosis and inappropriate use of steroids may compound morbidity.
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DOI: 10.1017/S0959259801011248
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In other words, the myopathies are those conditions in which the patient’s symptoms and signs can be attributed to a pathological process affecting either the structure of muscle fibres or their associated interstitial tissues, or to disturbance of the biochemical or electrophysiological function of those fibres. Myopathies are rare in all age ranges. They may be inherited or acquired. Onset of inherited myopathies in the elderly, not surprisingly, is uncommon, but some of these diseases are asymptomatic or cause such minor symptoms that their significance is not appreciated by the patient, and thus they may not be recognized until late on in life. Their recognition may have implications for other, younger, family members. Many of the acquired myopathies afflicting the elderly are treatable, but the commonest, inclusion body myositis, is not, and incorrect diagnosis and inappropriate use of steroids may compound morbidity.</div></front></TEI><istex><corpusName>cambridge</corpusName><author><json:item><name>David Hilton-Jones</name><affiliations><json:string>Radcliffe Infirmary,</json:string></affiliations></json:item></author><arkIstex>ark:/67375/6GQ-S6QVB0BT-D</arkIstex><language><json:string>eng</json:string></language><originalGenre><json:string>research-article</json:string></originalGenre><abstract>Myopathy is a convenient shorthand term meaning muscle disease or dysfunction. In other words, the myopathies are those conditions in which the patient’s symptoms and signs can be attributed to a pathological process affecting either the structure of muscle fibres or their associated interstitial tissues, or to disturbance of the biochemical or electrophysiological function of those fibres. Myopathies are rare in all age ranges. They may be inherited or acquired. Onset of inherited myopathies in the elderly, not surprisingly, is uncommon, but some of these diseases are asymptomatic or cause such minor symptoms that their significance is not appreciated by the patient, and thus they may not be recognized until late on in life. Their recognition may have implications for other, younger, family members. 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In other words, the myopathies are those conditions in which the patient’s symptoms and signs can be attributed to a pathological process affecting either the structure of muscle fibres or their associated interstitial tissues, or to disturbance of the biochemical or electrophysiological function of those fibres. Myopathies are rare in all age ranges. They may be inherited or acquired. Onset of inherited myopathies in the elderly, not surprisingly, is uncommon, but some of these diseases are asymptomatic or cause such minor symptoms that their significance is not appreciated by the patient, and thus they may not be recognized until late on in life. Their recognition may have implications for other, younger, family members. Many of the acquired myopathies afflicting the elderly are treatable, but the commonest, inclusion body myositis, is not, and incorrect diagnosis and inappropriate use of steroids may compound morbidity.</p></abstract></profileDesc><revisionDesc><change when="2001-10-18">Created</change><change when="2001-05">Published</change></revisionDesc></teiHeader></istex:fulltextTEI><json:item><extension>txt</extension><original>false</original><mimetype>text/plain</mimetype><uri>https://api.istex.fr/ark:/67375/6GQ-S6QVB0BT-D/fulltext.txt</uri></json:item></fulltext><metadata><istex:metadataXml wicri:clean="corpus cambridge not found" wicri:toSee="no header"><istex:xmlDeclaration>version='1.0' encoding='UTF-8'</istex:xmlDeclaration><istex:docType PUBLIC="-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.0 20120330//EN" URI="JATS-journalpublishing1.dtd" name="istex:docType"></istex:docType><istex:document><article dtd-version="1.0" article-type="research-article"><front><journal-meta><journal-id journal-id-type="publisher-id">RCG</journal-id><journal-title-group><journal-title>Reviews in Clinical Gerontology</journal-title><abbrev-journal-title>Rev. Clin. Gerontol.</abbrev-journal-title></journal-title-group><issn pub-type="epub">1469-9036</issn><issn pub-type="ppub">0959-2598</issn><publisher><publisher-name>Cambridge University Press</publisher-name><publisher-loc>Cambridge, UK</publisher-loc></publisher></journal-meta><article-meta><article-id pub-id-type="pii">S0959259801011248</article-id><article-id pub-id-type="doi">10.1017/S0959259801011248</article-id><article-categories><subj-group subj-group-type="heading"><subject>Occasional papers</subject></subj-group></article-categories><title-group><article-title>Myopathies</article-title></title-group><contrib-group><contrib><name><surname>Hilton-Jones</surname><given-names>David</given-names></name><aff><institution>Radcliffe Infirmary, </institution>Oxford, <country>UK</country>.</aff></contrib></contrib-group><pub-date pub-type="epub"><day>18</day><month>10</month><year>2001</year></pub-date><pub-date pub-type="ppub"><month>5</month><year>2001</year></pub-date><volume>11</volume><issue>2</issue><fpage>131</fpage><lpage>147</lpage><permissions><copyright-statement>© 2001 Cambridge University Press</copyright-statement></permissions><abstract abstract-type="text-abstract"><p>Myopathy is a convenient shorthand term meaning muscle disease or dysfunction.
In other words, the myopathies are those conditions in which the patient’s
symptoms and signs can be attributed to a pathological process affecting either the
structure of muscle fibres or their associated interstitial tissues, or to disturbance
of the biochemical or electrophysiological function of those fibres. Myopathies are
rare in all age ranges. They may be inherited or acquired. Onset of inherited myopathies
in the elderly, not surprisingly, is uncommon, but some of these diseases are asymptomatic
or cause such minor symptoms that their significance is not appreciated by the patient,
and thus they may not be recognized until late on in life. Their recognition may
have implications for other, younger, family members. Many of the acquired myopathies
afflicting the elderly are treatable, but the commonest, inclusion body myositis,
is not, and incorrect diagnosis and inappropriate use of steroids may compound morbidity.</p></abstract><counts><page-count count="17"></page-count></counts><custom-meta-group><custom-meta><meta-name>pdf</meta-name><meta-value>S0959259801011248a.pdf</meta-value></custom-meta></custom-meta-group></article-meta></front></article></istex:document></istex:metadataXml><mods version="3.6"><titleInfo><title>Myopathies</title></titleInfo><titleInfo type="alternative" contentType="CDATA"><title>Myopathies</title></titleInfo><name type="personal"><namePart type="given">David</namePart><namePart type="family">Hilton-Jones</namePart><affiliation>Radcliffe Infirmary,</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="research-article" displayLabel="research-article" authority="ISTEX" authorityURI="https://content-type.data.istex.fr" valueURI="https://content-type.data.istex.fr/ark:/67375/XTP-1JC4F85T-7">research-article</genre><originInfo><publisher>Cambridge University Press</publisher><place><placeTerm type="text">Cambridge, UK</placeTerm></place><dateIssued encoding="w3cdtf">2001-05</dateIssued><dateCreated encoding="w3cdtf">2001-10-18</dateCreated><copyrightDate encoding="w3cdtf">2001</copyrightDate></originInfo><language><languageTerm type="code" authority="iso639-2b">eng</languageTerm><languageTerm type="code" authority="rfc3066">en</languageTerm></language><abstract type="text-abstract">Myopathy is a convenient shorthand term meaning muscle disease or dysfunction. In other words, the myopathies are those conditions in which the patient’s symptoms and signs can be attributed to a pathological process affecting either the structure of muscle fibres or their associated interstitial tissues, or to disturbance of the biochemical or electrophysiological function of those fibres. Myopathies are rare in all age ranges. They may be inherited or acquired. Onset of inherited myopathies in the elderly, not surprisingly, is uncommon, but some of these diseases are asymptomatic or cause such minor symptoms that their significance is not appreciated by the patient, and thus they may not be recognized until late on in life. Their recognition may have implications for other, younger, family members. Many of the acquired myopathies afflicting the elderly are treatable, but the commonest, inclusion body myositis, is not, and incorrect diagnosis and inappropriate use of steroids may compound morbidity.</abstract><relatedItem type="host"><titleInfo><title>Reviews in Clinical Gerontology</title></titleInfo><genre type="journal" authority="ISTEX" authorityURI="https://publication-type.data.istex.fr" valueURI="https://publication-type.data.istex.fr/ark:/67375/JMC-0GLKJH51-B">journal</genre><identifier type="ISSN">0959-2598</identifier><identifier type="eISSN">1469-9036</identifier><identifier type="PublisherID">RCG</identifier><part><date>2001</date><detail type="volume"><caption>vol.</caption><number>11</number></detail><detail type="issue"><caption>no.</caption><number>2</number></detail><extent unit="pages"><start>131</start><end>147</end><total>17</total></extent></part></relatedItem><identifier type="istex">560373E0FC5E9D798CAC0D6F015C2221DC531903</identifier><identifier type="ark">ark:/67375/6GQ-S6QVB0BT-D</identifier><identifier type="DOI">10.1017/S0959259801011248</identifier><identifier type="PII">S0959259801011248</identifier><accessCondition type="use and reproduction" contentType="copyright">© 2001 Cambridge University Press</accessCondition><recordInfo><recordContentSource authority="ISTEX" authorityURI="https://loaded-corpus.data.istex.fr" valueURI="https://loaded-corpus.data.istex.fr/ark:/67375/XBH-G3RCRD03-V">cambridge</recordContentSource><recordOrigin>© 2001 Cambridge University Press</recordOrigin></recordInfo></mods><json:item><extension>json</extension><original>false</original><mimetype>application/json</mimetype><uri>https://api.istex.fr/ark:/67375/6GQ-S6QVB0BT-D/record.json</uri></json:item></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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