Familial parkinsonism with depression: A clinicopathological study
Identifieur interne : 000B82 ( Istex/Corpus ); précédent : 000B81; suivant : 000B83Familial parkinsonism with depression: A clinicopathological study
Auteurs : K Bhatia ; S Daniel ; MarsdenSource :
- Annals of Neurology [ 0364-5134 ] ; 1993-12.
Abstract
A family with autosomal dominant inheritance of an early‐onset and rapidly progressive parkinsonian syndrome and associated severe depression is reported. Three members had parkinsonism with depression, 3 had parkinsonism alone, and 2 suffered depression only. Pathological brain examination in 2 members with parkinsonism and depression revealed distinctive changes, with devastation of the substantia nigra, scarce Lewy bodies, and gliosis of the caudate nucleaus and globus pallidus. The clinical and pathological findings were similar to those in four previously described families with autosomal dominant parkinsonism, depression, and alveolar hypoventilation.
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DOI: 10.1002/ana.410340614
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Three members had parkinsonism with depression, 3 had parkinsonism alone, and 2 suffered depression only. Pathological brain examination in 2 members with parkinsonism and depression revealed distinctive changes, with devastation of the substantia nigra, scarce Lewy bodies, and gliosis of the caudate nucleaus and globus pallidus. The clinical and pathological findings were similar to those in four previously described families with autosomal dominant parkinsonism, depression, and alveolar hypoventilation.</div></front></TEI><istex><corpusName>wiley</corpusName><author><json:item><name>K. P. Bhatia MD, DM</name><affiliations><json:string>Department of Clinical Neurology and Parkinson's Disease Society Brain Bank, Queen Square, London, England</json:string><json:string>Institute of Neurology, National Hospital for Neurological Neurosurgery, Queen Square, London, England</json:string></affiliations></json:item><json:item><name>S. E. 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E.</forename><surname>Daniel</surname></persName><roleName type="degree">MD, MRCPath</roleName><affiliation>Department of Clinical Neurology and Parkinson's Disease Society Brain Bank, Queen Square, London, England</affiliation><affiliation>Institute of Neurology, National Hospital for Neurological Neurosurgery, Queen Square, London, England</affiliation></author><author><persName><surname>Marsden</surname></persName><roleName type="degree">Prof.</roleName><note type="correspondence"><p>Correspondence: Institute of Neurology, Queen Square, London, WC1N 3BG UK</p></note><affiliation>Department of Clinical Neurology and Parkinson's Disease Society Brain Bank, Queen Square, London, England</affiliation><affiliation>Institute of Neurology, National Hospital for Neurological Neurosurgery, Queen Square, London, England</affiliation></author></analytic><monogr><title level="j">Annals of Neurology</title><title level="j" type="sub">Official Journal of the American Neurological Association and the Child Neurology Society</title><title level="j" type="abbrev">Ann Neurol.</title><idno type="pISSN">0364-5134</idno><idno type="eISSN">1531-8249</idno><idno type="DOI">10.1002/(ISSN)1531-8249</idno><imprint><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><pubPlace>Hoboken</pubPlace><date type="published" when="1993-12"></date><biblScope unit="volume">34</biblScope><biblScope unit="issue">6</biblScope><biblScope unit="page" from="842">842</biblScope><biblScope unit="page" to="847">847</biblScope></imprint></monogr><idno type="istex">66E01E9144ECADD3F19EEDCCCE65F0A61401BB16</idno><idno type="DOI">10.1002/ana.410340614</idno><idno type="ArticleID">ANA410340614</idno></biblStruct></sourceDesc></fileDesc><profileDesc><creation><date>1993</date></creation><langUsage><language ident="en">en</language></langUsage><abstract xml:lang="en"><p>A family with autosomal dominant inheritance of an early‐onset and rapidly progressive parkinsonian syndrome and associated severe depression is reported. 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D.</givenNames><familyName>Marsden</familyName><degrees>FRS</degrees></personName></creator></creators><affiliationGroup><affiliation xml:id="af1" countryCode="GB" type="organization"><unparsedAffiliation>Department of Clinical Neurology and Parkinson's Disease Society Brain Bank, Queen Square, London, England</unparsedAffiliation></affiliation><affiliation xml:id="af2" countryCode="GB" type="organization"><unparsedAffiliation>Institute of Neurology, National Hospital for Neurological Neurosurgery, Queen Square, London, England</unparsedAffiliation></affiliation></affiliationGroup><abstractGroup><abstract type="main" xml:lang="en"><title type="main">Abstract</title><p>A family with autosomal dominant inheritance of an early‐onset and rapidly progressive parkinsonian syndrome and associated severe depression is reported. Three members had parkinsonism with depression, 3 had parkinsonism alone, and 2 suffered depression only. Pathological brain examination in 2 members with parkinsonism and depression revealed distinctive changes, with devastation of the substantia nigra, scarce Lewy bodies, and gliosis of the caudate nucleaus and globus pallidus. The clinical and pathological findings were similar to those in four previously described families with autosomal dominant parkinsonism, depression, and alveolar hypoventilation.</p></abstract></abstractGroup></contentMeta></header></component></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Familial parkinsonism with depression: A clinicopathological study</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>Familial Parkinsonism with Depression</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Familial parkinsonism with depression: A clinicopathological study</title></titleInfo><name type="personal"><namePart type="given">K. 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Three members had parkinsonism with depression, 3 had parkinsonism alone, and 2 suffered depression only. Pathological brain examination in 2 members with parkinsonism and depression revealed distinctive changes, with devastation of the substantia nigra, scarce Lewy bodies, and gliosis of the caudate nucleaus and globus pallidus. The clinical and pathological findings were similar to those in four previously described families with autosomal dominant parkinsonism, depression, and alveolar hypoventilation.</abstract><relatedItem type="host"><titleInfo><title>Annals of Neurology</title><subTitle>Official Journal of the American Neurological Association and the Child Neurology Society</subTitle></titleInfo><titleInfo type="abbreviated"><title>Ann Neurol.</title></titleInfo><subject><genre>article category</genre><topic>Original Article</topic></subject><identifier type="ISSN">0364-5134</identifier><identifier type="eISSN">1531-8249</identifier><identifier type="DOI">10.1002/(ISSN)1531-8249</identifier><identifier type="PublisherID">ANA</identifier><part><date>1993</date><detail type="volume"><caption>vol.</caption><number>34</number></detail><detail type="issue"><caption>no.</caption><number>6</number></detail><extent unit="pages"><start>842</start><end>847</end><total>6</total></extent></part></relatedItem><identifier type="istex">66E01E9144ECADD3F19EEDCCCE65F0A61401BB16</identifier><identifier type="DOI">10.1002/ana.410340614</identifier><identifier type="ArticleID">ANA410340614</identifier><accessCondition type="use and reproduction" contentType="copyright">Copyright © 1993 American Neurological Association</accessCondition><recordInfo><recordOrigin>Wiley Subscription Services, Inc., A Wiley Company</recordOrigin><recordContentSource>WILEY</recordContentSource></recordInfo></mods></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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