MovDisordV3, Main, Exploration, bibRecord, 003A61

Preserved myocardial [123I]metaiodobenzylguanidine uptake in autosomal recessive juvenile parkinsonism : First case report

Identifieur interne : 003A61 ( Main/Exploration ); précédent : 003A60; suivant : 003A62

Preserved myocardial [123I]metaiodobenzylguanidine uptake in autosomal recessive juvenile parkinsonism : First case report

Auteurs : Masahiko Suzuki [Japon] ; Nobutaka Hattori [Japon] ; Satoshi Orimo [Japon] ; Nobuyoshi Fukumitsu [Japon] ; M. Masahiro Abo [Japon] ; Yu Kono [Japon] ; Renpei Sengoku [Japon] ; Akira Kurita [Japon] ; Hidehiko Honda [Japon] ; Kiyoharu Inoue [Japon]

Source :

Movement disorders [ 0885-3185 ] ; 2005.

RBID : Pascal:05-0281352

Descripteurs français

Pascal (Inist)
- Système nerveux pathologie, Parkinsonisme, Parkinson maladie, Captation, Etude cas.

English descriptors

KwdEn :
- Case study, Nervous system diseases, Parkinson disease, Parkinsonism, Uptake.

Abstract

A decrease in myocardial uptake of iodine-123-labeled metaiodobenzylguanidine (¹²³I-MIBG) has been reported in idiopathic Parkinson's disease (PD) using ¹²³I-MIBG myocardial scintigraphy. However, the patient with autosomal recessive juvenile parkinsonism (AR-JP). caused by the parkin gene, presented here showed normal ¹²³I-MIBG myocardial uptake, suggesting that AR-JP is a distinct disease entity from PD. Although the clinical features of AR-JP are sometimes quite similar to those of late-onset idiopathic PD. ¹²³I-MISG myocardial scintigraphy may be a powerful tool to differentiate PD from other parkinsonian syndromes, including AR-JP.

Affiliations:

Japon
Tokyo

Links toward previous steps (curation, corpus...)

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to stream PascalFrancis, to step Curation: 000E38
to stream PascalFrancis, to step Checkpoint: 001D46
to stream Main, to step Merge: 005224
to stream Main, to step Curation: 003A61

Le document en format XML

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<author><name sortKey="Kurita, Akira" sort="Kurita, Akira" uniqKey="Kurita A" first="Akira" last="Kurita">Akira Kurita</name>
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<author><name sortKey="Honda, Hidehiko" sort="Honda, Hidehiko" uniqKey="Honda H" first="Hidehiko" last="Honda">Hidehiko Honda</name>
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">Preserved myocardial [<sup>123</sup>
I]metaiodobenzylguanidine uptake in autosomal recessive juvenile parkinsonism : First case report</title>
<author><name sortKey="Suzuki, Masahiko" sort="Suzuki, Masahiko" uniqKey="Suzuki M" first="Masahiko" last="Suzuki">Masahiko Suzuki</name>
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<sZ>6 aut.</sZ>
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</affiliation>
</author>
<author><name sortKey="Sengoku, Renpei" sort="Sengoku, Renpei" uniqKey="Sengoku R" first="Renpei" last="Sengoku">Renpei Sengoku</name>
<affiliation wicri:level="3"><inist:fA14 i1="01"><s1>Department of Neurology, The Jikei University School of Medicine</s1>
<s2>Tokyo</s2>
<s3>JPN</s3>
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</author>
<author><name sortKey="Kurita, Akira" sort="Kurita, Akira" uniqKey="Kurita A" first="Akira" last="Kurita">Akira Kurita</name>
<affiliation wicri:level="3"><inist:fA14 i1="01"><s1>Department of Neurology, The Jikei University School of Medicine</s1>
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<s3>JPN</s3>
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</author>
<author><name sortKey="Honda, Hidehiko" sort="Honda, Hidehiko" uniqKey="Honda H" first="Hidehiko" last="Honda">Hidehiko Honda</name>
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</inist:fA14>
<country>Japon</country>
<placeName><settlement type="city">Tokyo</settlement>
</placeName>
</affiliation>
</author>
<author><name sortKey="Inoue, Kiyoharu" sort="Inoue, Kiyoharu" uniqKey="Inoue K" first="Kiyoharu" last="Inoue">Kiyoharu Inoue</name>
<affiliation wicri:level="3"><inist:fA14 i1="01"><s1>Department of Neurology, The Jikei University School of Medicine</s1>
<s2>Tokyo</s2>
<s3>JPN</s3>
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<country>Japon</country>
<placeName><settlement type="city">Tokyo</settlement>
</placeName>
</affiliation>
</author>
</analytic>
<series><title level="j" type="main">Movement disorders</title>
<title level="j" type="abbreviated">Mov. disord.</title>
<idno type="ISSN">0885-3185</idno>
<imprint><date when="2005">2005</date>
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<idno type="ISSN">0885-3185</idno>
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</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Case study</term>
<term>Nervous system diseases</term>
<term>Parkinson disease</term>
<term>Parkinsonism</term>
<term>Uptake</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Système nerveux pathologie</term>
<term>Parkinsonisme</term>
<term>Parkinson maladie</term>
<term>Captation</term>
<term>Etude cas</term>
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<front><div type="abstract" xml:lang="en">A decrease in myocardial uptake of iodine-123-labeled metaiodobenzylguanidine (<sup>123</sup>
I-MIBG) has been reported in idiopathic Parkinson's disease (PD) using <sup>123</sup>
I-MIBG myocardial scintigraphy. However, the patient with autosomal recessive juvenile parkinsonism (AR-JP). caused by the parkin gene, presented here showed normal <sup>123</sup>
I-MIBG myocardial uptake, suggesting that AR-JP is a distinct disease entity from PD. Although the clinical features of AR-JP are sometimes quite similar to those of late-onset idiopathic PD. <sup>123</sup>
I-MISG myocardial scintigraphy may be a powerful tool to differentiate PD from other parkinsonian syndromes, including AR-JP.</div>
</front>
</TEI>
<affiliations><list><country><li>Japon</li>
</country>
<settlement><li>Tokyo</li>
</settlement>
</list>
<tree><country name="Japon"><noRegion><name sortKey="Suzuki, Masahiko" sort="Suzuki, Masahiko" uniqKey="Suzuki M" first="Masahiko" last="Suzuki">Masahiko Suzuki</name>
</noRegion>
<name sortKey="Fukumitsu, Nobuyoshi" sort="Fukumitsu, Nobuyoshi" uniqKey="Fukumitsu N" first="Nobuyoshi" last="Fukumitsu">Nobuyoshi Fukumitsu</name>
<name sortKey="Hattori, Nobutaka" sort="Hattori, Nobutaka" uniqKey="Hattori N" first="Nobutaka" last="Hattori">Nobutaka Hattori</name>
<name sortKey="Honda, Hidehiko" sort="Honda, Hidehiko" uniqKey="Honda H" first="Hidehiko" last="Honda">Hidehiko Honda</name>
<name sortKey="Inoue, Kiyoharu" sort="Inoue, Kiyoharu" uniqKey="Inoue K" first="Kiyoharu" last="Inoue">Kiyoharu Inoue</name>
<name sortKey="Kono, Yu" sort="Kono, Yu" uniqKey="Kono Y" first="Yu" last="Kono">Yu Kono</name>
<name sortKey="Kurita, Akira" sort="Kurita, Akira" uniqKey="Kurita A" first="Akira" last="Kurita">Akira Kurita</name>
<name sortKey="Masahiro Abo, M" sort="Masahiro Abo, M" uniqKey="Masahiro Abo M" first="M." last="Masahiro Abo">M. Masahiro Abo</name>
<name sortKey="Orimo, Satoshi" sort="Orimo, Satoshi" uniqKey="Orimo S" first="Satoshi" last="Orimo">Satoshi Orimo</name>
<name sortKey="Sengoku, Renpei" sort="Sengoku, Renpei" uniqKey="Sengoku R" first="Renpei" last="Sengoku">Renpei Sengoku</name>
</country>
</tree>
</affiliations>
</record>

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	Movement Disorders (revue)
	Attention, ce site est en cours de développement ! Attention, site généré par des moyens informatiques à partir de corpus bruts. Les informations ne sont donc pas validées.

Movement Disorders (revue)

Preserved myocardial [123I]metaiodobenzylguanidine uptake in autosomal recessive juvenile parkinsonism : First case report

Preserved myocardial [123I]metaiodobenzylguanidine uptake in autosomal recessive juvenile parkinsonism : First case report

Source :

Descripteurs français

English descriptors

Abstract

Links toward previous steps (curation, corpus...)

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri