Hereditary spastic paraplegia associated with dopa‐responsive parkinsonism
Identifieur interne : 003405 ( Main/Exploration ); précédent : 003404; suivant : 003406Hereditary spastic paraplegia associated with dopa‐responsive parkinsonism
Auteurs : Federico Micheli [Argentine] ; María Graciela Cers Simo [Argentine] ; Carlos Zú Iga Ramírez [Argentine]Source :
- Movement Disorders [ 0885-3185 ] ; 2006-05.
Descripteurs français
- Pascal (Inist)
English descriptors
- KwdEn :
- Antiparkinson Agents (therapeutic use), Dopa, Follow-Up Studies, Hereditary spastic paraplegia, Humans, Levodopa, Levodopa (therapeutic use), Male, Middle Aged, Nervous system diseases, Paraparesia, Parkinson Disease (drug therapy), Parkinson Disease (etiology), Parkinsonism, Spastic Paraplegia, Hereditary (complications), Spastic Paraplegia, Hereditary (drug therapy), levodopa, paraparesis.
- MESH :
- chemical , therapeutic use : Antiparkinson Agents, Levodopa.
- complications : Spastic Paraplegia, Hereditary.
- drug therapy : Parkinson Disease, Spastic Paraplegia, Hereditary.
- etiology : Parkinson Disease.
- Follow-Up Studies, Humans, Male, Middle Aged.
Abstract
A 47‐year‐old patient with hereditary spastic paraplegia and parkinsonian features is reported. Treatment with levodopa led to marked improvement in his neurological status and quality of life. However, several years later he developed motor fluctuations and dyskinesias. The latter promptly remitted with amantadine treatment. © 2006 Movement Disorder Society
Url:
DOI: 10.1002/mds.20800
Affiliations:
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Le document en format XML
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Disord.</title><idno type="ISSN">0885-3185</idno><idno type="eISSN">1531-8257</idno><imprint><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><pubPlace>Hoboken</pubPlace><date type="published" when="2006-05">2006-05</date><biblScope unit="vol">21</biblScope><biblScope unit="issue">5</biblScope><biblScope unit="page" from="716">716</biblScope><biblScope unit="page" to="717">717</biblScope></imprint><idno type="ISSN">0885-3185</idno></series><idno type="istex">2E301B3433AD4B9F6B9532DDCFA022A3AAC309CA</idno><idno type="DOI">10.1002/mds.20800</idno><idno type="ArticleID">MDS20800</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0885-3185</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Antiparkinson Agents (therapeutic use)</term><term>Dopa</term><term>Follow-Up Studies</term><term>Hereditary spastic paraplegia</term><term>Humans</term><term>Levodopa</term><term>Levodopa (therapeutic use)</term><term>Male</term><term>Middle Aged</term><term>Nervous system diseases</term><term>Paraparesia</term><term>Parkinson Disease (drug therapy)</term><term>Parkinson Disease (etiology)</term><term>Parkinsonism</term><term>Spastic Paraplegia, Hereditary (complications)</term><term>Spastic Paraplegia, Hereditary (drug therapy)</term><term>levodopa</term><term>paraparesis</term></keywords><keywords scheme="MESH" type="chemical" qualifier="therapeutic use" xml:lang="en"><term>Antiparkinson Agents</term><term>Levodopa</term></keywords><keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Spastic Paraplegia, Hereditary</term></keywords><keywords scheme="MESH" qualifier="drug therapy" xml:lang="en"><term>Parkinson Disease</term><term>Spastic Paraplegia, Hereditary</term></keywords><keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Parkinson Disease</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Follow-Up Studies</term><term>Humans</term><term>Male</term><term>Middle Aged</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Dopa</term><term>Lévodopa</term><term>Paraparésie</term><term>Paraplégie spasmodique héréditaire Strumpell Lorrain</term><term>Parkinsonisme</term><term>Système nerveux pathologie</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">A 47‐year‐old patient with hereditary spastic paraplegia and parkinsonian features is reported. Treatment with levodopa led to marked improvement in his neurological status and quality of life. However, several years later he developed motor fluctuations and dyskinesias. The latter promptly remitted with amantadine treatment. © 2006 Movement Disorder Society</div></front></TEI><affiliations><list><country><li>Argentine</li></country></list><tree><country name="Argentine"><noRegion><name sortKey="Micheli, Federico" sort="Micheli, Federico" uniqKey="Micheli F" first="Federico" last="Micheli">Federico Micheli</name></noRegion><name sortKey="Cers Simo, Maria Graciela" sort="Cers Simo, Maria Graciela" uniqKey="Cers Simo M" first="María Graciela" last="Cers Simo">María Graciela Cers Simo</name><name sortKey="Zu Iga Ramirez, Carlos" sort="Zu Iga Ramirez, Carlos" uniqKey="Zu Iga Ramirez C" first="Carlos" last="Zú Iga Ramírez">Carlos Zú Iga Ramírez</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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