Pediatric multiple sclerosis report of 14 cases
We present clinical data from 14 multiple sclerosis (MS) patients who have been admitted to our hospital between January 1980 and May 1992, whose age of onset ranged from 2–15 years. Our patients could be classified as having a clinically definite form of the disease. Initial symptoms varied from mi...
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Veröffentlicht in: | Brain & development (Tokyo. 1979) 1995, Vol.17 (1), p.9-12 |
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creator | de Figueiredo Ferreira Guilhoto, Laura Maria Martinez Osório, Carlos Alberto Machado, Lúcia Ribeiro de Castro, Cleise Pereira Giraldes Manreza, Maria Luíza Callegaro, Dagoberto Kok, Fernando Diament, Aron |
description | We present clinical data from 14 multiple sclerosis (MS) patients who have been admitted to our hospital between January 1980 and May 1992, whose age of onset ranged from 2–15 years. Our patients could be classified as having a clinically definite form of the disease. Initial symptoms varied from minor, such as motor or sensory impairment, bladder dysfunction, to the worst clinical presentation, suggesting diffuse encephalopathy. All the patients had a relapsing-remitting course. We report the paraclinical and laboratory examinations that were done in these patients. Over the period 1980 to 1992 these patients had 39 attacks. CSF analysis was performed in the phase of activity of the disease on 23 occasions and was normal in 12. At least one brain CT scan was performed in 9 patients and showed white matter abnormalities in 6. Cranial magnetic resonance imaging was done in 6 patients and were abnormal in 5. Visual evoked potential (EP) was abnormal in 7 of 8 patients; brainstem acoustic EP was abnormal in 4 of 8 patients and somatosensory EP in 4 of 8. MS is not so rare in childhood and although its diagnosis is essentially a clinical one, paraclinical investigations are of great value in the identification of demyelinating disorders in childhood. |
doi_str_mv | 10.1016/0387-7604(94)00091-B |
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Our patients could be classified as having a clinically definite form of the disease. Initial symptoms varied from minor, such as motor or sensory impairment, bladder dysfunction, to the worst clinical presentation, suggesting diffuse encephalopathy. All the patients had a relapsing-remitting course. We report the paraclinical and laboratory examinations that were done in these patients. Over the period 1980 to 1992 these patients had 39 attacks. CSF analysis was performed in the phase of activity of the disease on 23 occasions and was normal in 12. At least one brain CT scan was performed in 9 patients and showed white matter abnormalities in 6. Cranial magnetic resonance imaging was done in 6 patients and were abnormal in 5. Visual evoked potential (EP) was abnormal in 7 of 8 patients; brainstem acoustic EP was abnormal in 4 of 8 patients and somatosensory EP in 4 of 8. MS is not so rare in childhood and although its diagnosis is essentially a clinical one, paraclinical investigations are of great value in the identification of demyelinating disorders in childhood.</description><identifier>ISSN: 0387-7604</identifier><identifier>EISSN: 1872-7131</identifier><identifier>DOI: 10.1016/0387-7604(94)00091-B</identifier><identifier>PMID: 7762771</identifier><identifier>CODEN: NTHAA7</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Adolescent ; Age of Onset ; Biological and medical sciences ; Brain - pathology ; Cerebrospinal Fluid - chemistry ; Child ; Child, Preschool ; Demyelinating disease ; Evoked Potentials, Visual - physiology ; Female ; Humans ; Magnetic Resonance Imaging ; Male ; Medical sciences ; Multiple sclerosis ; Multiple Sclerosis - classification ; Multiple Sclerosis - diagnosis ; Multiple Sclerosis - physiopathology ; Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis ; Neurology</subject><ispartof>Brain & development (Tokyo. 1979), 1995, Vol.17 (1), p.9-12</ispartof><rights>1995 Elsevier Science B.V. All rights reserved</rights><rights>1995 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c415t-eb175b7d4eee87970c8230bad1f64c1ae435a300b4899cb08caaa8af283482883</citedby><cites>FETCH-LOGICAL-c415t-eb175b7d4eee87970c8230bad1f64c1ae435a300b4899cb08caaa8af283482883</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/0387-7604(94)00091-B$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,4024,27923,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3544522$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7762771$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>de Figueiredo Ferreira Guilhoto, Laura Maria</creatorcontrib><creatorcontrib>Martinez Osório, Carlos Alberto</creatorcontrib><creatorcontrib>Machado, Lúcia Ribeiro</creatorcontrib><creatorcontrib>de Castro, Cleise Pereira</creatorcontrib><creatorcontrib>Giraldes Manreza, Maria Luíza</creatorcontrib><creatorcontrib>Callegaro, Dagoberto</creatorcontrib><creatorcontrib>Kok, Fernando</creatorcontrib><creatorcontrib>Diament, Aron</creatorcontrib><title>Pediatric multiple sclerosis report of 14 cases</title><title>Brain & development (Tokyo. 1979)</title><addtitle>Brain Dev</addtitle><description>We present clinical data from 14 multiple sclerosis (MS) patients who have been admitted to our hospital between January 1980 and May 1992, whose age of onset ranged from 2–15 years. Our patients could be classified as having a clinically definite form of the disease. Initial symptoms varied from minor, such as motor or sensory impairment, bladder dysfunction, to the worst clinical presentation, suggesting diffuse encephalopathy. All the patients had a relapsing-remitting course. We report the paraclinical and laboratory examinations that were done in these patients. Over the period 1980 to 1992 these patients had 39 attacks. CSF analysis was performed in the phase of activity of the disease on 23 occasions and was normal in 12. At least one brain CT scan was performed in 9 patients and showed white matter abnormalities in 6. Cranial magnetic resonance imaging was done in 6 patients and were abnormal in 5. Visual evoked potential (EP) was abnormal in 7 of 8 patients; brainstem acoustic EP was abnormal in 4 of 8 patients and somatosensory EP in 4 of 8. MS is not so rare in childhood and although its diagnosis is essentially a clinical one, paraclinical investigations are of great value in the identification of demyelinating disorders in childhood.</description><subject>Adolescent</subject><subject>Age of Onset</subject><subject>Biological and medical sciences</subject><subject>Brain - pathology</subject><subject>Cerebrospinal Fluid - chemistry</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Demyelinating disease</subject><subject>Evoked Potentials, Visual - physiology</subject><subject>Female</subject><subject>Humans</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Multiple sclerosis</subject><subject>Multiple Sclerosis - classification</subject><subject>Multiple Sclerosis - diagnosis</subject><subject>Multiple Sclerosis - physiopathology</subject><subject>Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis</subject><subject>Neurology</subject><issn>0387-7604</issn><issn>1872-7131</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1LxDAURYMo4zj6DxS6ENFFnbwkbZKN4Ax-wYAudB3S9BUi7XRMWsF_b8cps3T1Fvfcy-MQcg70Fijkc8qVTGVOxbUWN5RSDenigExBSZZK4HBIpnvkmJzE-DlAwIBOyETKnEkJUzJ_w9LbLniXNH3d-U2NSXQ1hjb6mATctKFL2ioBkTgbMZ6So8rWEc_GOyMfjw_vy-d09fr0srxfpU5A1qVYgMwKWQpEVFJL6hTjtLAlVLlwYFHwzHJKC6G0dgVVzlqrbMUUF4opxWfkare7Ce1Xj7EzjY8O69quse2jkZJpoVU-gGIHuuHlGLAym-AbG34MULP1ZLYSzFaC0cL8eTKLoXYx7vdFg-W-NIoZ8ssxt9HZugp27XzcYzwTImNswO52GA4uvj0GE53HtRukBnSdKVv__x-_AdeCTg</recordid><startdate>1995</startdate><enddate>1995</enddate><creator>de Figueiredo Ferreira Guilhoto, Laura Maria</creator><creator>Martinez Osório, Carlos Alberto</creator><creator>Machado, Lúcia Ribeiro</creator><creator>de Castro, Cleise Pereira</creator><creator>Giraldes Manreza, Maria Luíza</creator><creator>Callegaro, Dagoberto</creator><creator>Kok, Fernando</creator><creator>Diament, Aron</creator><general>Elsevier B.V</general><general>Elsevier Science</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>8BM</scope></search><sort><creationdate>1995</creationdate><title>Pediatric multiple sclerosis report of 14 cases</title><author>de Figueiredo Ferreira Guilhoto, Laura Maria ; Martinez Osório, Carlos Alberto ; Machado, Lúcia Ribeiro ; de Castro, Cleise Pereira ; Giraldes Manreza, Maria Luíza ; Callegaro, Dagoberto ; Kok, Fernando ; Diament, Aron</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c415t-eb175b7d4eee87970c8230bad1f64c1ae435a300b4899cb08caaa8af283482883</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Adolescent</topic><topic>Age of Onset</topic><topic>Biological and medical sciences</topic><topic>Brain - pathology</topic><topic>Cerebrospinal Fluid - chemistry</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Demyelinating disease</topic><topic>Evoked Potentials, Visual - physiology</topic><topic>Female</topic><topic>Humans</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Multiple sclerosis</topic><topic>Multiple Sclerosis - classification</topic><topic>Multiple Sclerosis - diagnosis</topic><topic>Multiple Sclerosis - physiopathology</topic><topic>Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis</topic><topic>Neurology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>de Figueiredo Ferreira Guilhoto, Laura Maria</creatorcontrib><creatorcontrib>Martinez Osório, Carlos Alberto</creatorcontrib><creatorcontrib>Machado, Lúcia Ribeiro</creatorcontrib><creatorcontrib>de Castro, Cleise Pereira</creatorcontrib><creatorcontrib>Giraldes Manreza, Maria Luíza</creatorcontrib><creatorcontrib>Callegaro, Dagoberto</creatorcontrib><creatorcontrib>Kok, Fernando</creatorcontrib><creatorcontrib>Diament, Aron</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>ComDisDome</collection><jtitle>Brain & development (Tokyo. 1979)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>de Figueiredo Ferreira Guilhoto, Laura Maria</au><au>Martinez Osório, Carlos Alberto</au><au>Machado, Lúcia Ribeiro</au><au>de Castro, Cleise Pereira</au><au>Giraldes Manreza, Maria Luíza</au><au>Callegaro, Dagoberto</au><au>Kok, Fernando</au><au>Diament, Aron</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pediatric multiple sclerosis report of 14 cases</atitle><jtitle>Brain & development (Tokyo. 1979)</jtitle><addtitle>Brain Dev</addtitle><date>1995</date><risdate>1995</risdate><volume>17</volume><issue>1</issue><spage>9</spage><epage>12</epage><pages>9-12</pages><issn>0387-7604</issn><eissn>1872-7131</eissn><coden>NTHAA7</coden><abstract>We present clinical data from 14 multiple sclerosis (MS) patients who have been admitted to our hospital between January 1980 and May 1992, whose age of onset ranged from 2–15 years. Our patients could be classified as having a clinically definite form of the disease. Initial symptoms varied from minor, such as motor or sensory impairment, bladder dysfunction, to the worst clinical presentation, suggesting diffuse encephalopathy. All the patients had a relapsing-remitting course. We report the paraclinical and laboratory examinations that were done in these patients. Over the period 1980 to 1992 these patients had 39 attacks. CSF analysis was performed in the phase of activity of the disease on 23 occasions and was normal in 12. At least one brain CT scan was performed in 9 patients and showed white matter abnormalities in 6. Cranial magnetic resonance imaging was done in 6 patients and were abnormal in 5. Visual evoked potential (EP) was abnormal in 7 of 8 patients; brainstem acoustic EP was abnormal in 4 of 8 patients and somatosensory EP in 4 of 8. 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subjects | Adolescent Age of Onset Biological and medical sciences Brain - pathology Cerebrospinal Fluid - chemistry Child Child, Preschool Demyelinating disease Evoked Potentials, Visual - physiology Female Humans Magnetic Resonance Imaging Male Medical sciences Multiple sclerosis Multiple Sclerosis - classification Multiple Sclerosis - diagnosis Multiple Sclerosis - physiopathology Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis Neurology |
title | Pediatric multiple sclerosis report of 14 cases |
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