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Lissencephaly-Pachygyria Associated With Congenital Cytomegalovirus Infection
We report the presence of major cerebral migrational defects in five severely, multiply handicapped children with congenital cytomegalovirus (CMV) infection. These patients had both computed tomographic (CT) scan and magnetic resonance imaging (MRI) evidence of marked migrational central nervous sys...
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Published in: | Journal of child neurology 1991-04, Vol.6 (2), p.109-114 |
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description | We report the presence of major cerebral migrational defects in five severely, multiply handicapped children with congenital cytomegalovirus (CMV) infection. These patients had both computed tomographic (CT) scan and magnetic resonance imaging (MRI) evidence of marked migrational central nervous system defects consistent anatomically with the spectrum of lissencephaly-pachygyria, a disorder commonly idiopathic or associated with chromosomal abnormalities or with unknown early gestational insults. Neuroradiologic features included broad, flat gyri, shallow sulci, incomplete opercularization, ventriculomegaly, periventricular calcifications, and white-matter hypodensity on CT scans or increased signal intensity on long-TR MRI scans. Evidence for congenital CMV infection included prenatal onset of microcephaly, periventricular calcifications, neonatal jaundice, hepatomegaly, elevated CMV-specific immunoglobulin M, or viral isolation from urine. Previous reports of the neurologic sequelae of CMV have emphasized varying degrees of psychomotor retardation, cerebral palsy and epilepsy due to polymicrogyria, periventricular calcification, microcephaly, or rarely, hydrocephalus. Our patients appear to represent extremely severe examples of the effects of CMV on neurologic growth, maturation, and development. Recognition of these severe migrational abnormalities was improved by use of MRI, a technique that affords superior definition of the nature and extent of gyral and white-matter abnormalities. We suggest that these abnormalities may be more common than has previously been recognized. (J Child Neurol 1991;6:109-114). |
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These patients had both computed tomographic (CT) scan and magnetic resonance imaging (MRI) evidence of marked migrational central nervous system defects consistent anatomically with the spectrum of lissencephaly-pachygyria, a disorder commonly idiopathic or associated with chromosomal abnormalities or with unknown early gestational insults. Neuroradiologic features included broad, flat gyri, shallow sulci, incomplete opercularization, ventriculomegaly, periventricular calcifications, and white-matter hypodensity on CT scans or increased signal intensity on long-TR MRI scans. Evidence for congenital CMV infection included prenatal onset of microcephaly, periventricular calcifications, neonatal jaundice, hepatomegaly, elevated CMV-specific immunoglobulin M, or viral isolation from urine. Previous reports of the neurologic sequelae of CMV have emphasized varying degrees of psychomotor retardation, cerebral palsy and epilepsy due to polymicrogyria, periventricular calcification, microcephaly, or rarely, hydrocephalus. Our patients appear to represent extremely severe examples of the effects of CMV on neurologic growth, maturation, and development. Recognition of these severe migrational abnormalities was improved by use of MRI, a technique that affords superior definition of the nature and extent of gyral and white-matter abnormalities. We suggest that these abnormalities may be more common than has previously been recognized. 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These patients had both computed tomographic (CT) scan and magnetic resonance imaging (MRI) evidence of marked migrational central nervous system defects consistent anatomically with the spectrum of lissencephaly-pachygyria, a disorder commonly idiopathic or associated with chromosomal abnormalities or with unknown early gestational insults. Neuroradiologic features included broad, flat gyri, shallow sulci, incomplete opercularization, ventriculomegaly, periventricular calcifications, and white-matter hypodensity on CT scans or increased signal intensity on long-TR MRI scans. Evidence for congenital CMV infection included prenatal onset of microcephaly, periventricular calcifications, neonatal jaundice, hepatomegaly, elevated CMV-specific immunoglobulin M, or viral isolation from urine. Previous reports of the neurologic sequelae of CMV have emphasized varying degrees of psychomotor retardation, cerebral palsy and epilepsy due to polymicrogyria, periventricular calcification, microcephaly, or rarely, hydrocephalus. Our patients appear to represent extremely severe examples of the effects of CMV on neurologic growth, maturation, and development. Recognition of these severe migrational abnormalities was improved by use of MRI, a technique that affords superior definition of the nature and extent of gyral and white-matter abnormalities. We suggest that these abnormalities may be more common than has previously been recognized. (J Child Neurol 1991;6:109-114).</description><subject>Atrophy - pathology</subject><subject>Brain - abnormalities</subject><subject>Brain - pathology</subject><subject>Brain Diseases - complications</subject><subject>Brain Diseases - congenital</subject><subject>Brain Diseases - diagnosis</subject><subject>Brain Diseases - diagnostic imaging</subject><subject>Calcinosis - pathology</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Cytomegalovirus</subject><subject>Cytomegalovirus Infections - complications</subject><subject>Cytomegalovirus Infections - congenital</subject><subject>Female</subject><subject>Humans</subject><subject>Infant</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Retrospective Studies</subject><subject>Tomography, X-Ray Computed</subject><issn>0883-0738</issn><issn>1708-8283</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><recordid>eNqFkM1Kw0AURgdRaq2-gCBk5S72zkwzmSxL8KdQ0YXiMkwyN-mUJFMziZC3NyEFF4Ku7uKe8y0OIdcU7igNwyVIySHkMqIAAoABPyFzGoL0JZP8lMxHwB-Jc3Lh3B4AZBDBjMyoWAkW8Dl53hrnsM7wsFNl77-qbNcXfWOUt3bOZka1qL0P0-682NYF1qZVpRf3ra2wUKX9Mk3nvE2dY9YaW1-Ss1yVDq-Od0HeH-7f4id_-_K4iddbP-Mian0hM52joirUYQCpXmnMmaaCCaojlutQrJDnFLSANNU61WL0IspT1IMh-ILcTruHxn526NqkMi7DslQ12s4lcsgRMh78CzI6RJORHEA2gVljnWswTw6NqVTTJxSSMXbyO_Yg3RzXu7RC_aNMdYf_cvo7VWCyt11TD1X-WvwG7DiIeg</recordid><startdate>19910401</startdate><enddate>19910401</enddate><creator>Hayward, Jean C.</creator><creator>Titelbaum, David S.</creator><creator>Clancy, Robert R.</creator><creator>Zimmerman, Robert A.</creator><general>Sage Publications</general><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>7TK</scope><scope>7U9</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>19910401</creationdate><title>Lissencephaly-Pachygyria Associated With Congenital Cytomegalovirus Infection</title><author>Hayward, Jean C. ; Titelbaum, David S. ; Clancy, Robert R. ; Zimmerman, Robert A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c369t-68cdfea1a7d750bd4def2d16261d92fd764e3f10d60bbddbd6c369913bedd7563</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>Atrophy - pathology</topic><topic>Brain - abnormalities</topic><topic>Brain - pathology</topic><topic>Brain Diseases - complications</topic><topic>Brain Diseases - congenital</topic><topic>Brain Diseases - diagnosis</topic><topic>Brain Diseases - diagnostic imaging</topic><topic>Calcinosis - pathology</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Cytomegalovirus</topic><topic>Cytomegalovirus Infections - complications</topic><topic>Cytomegalovirus Infections - congenital</topic><topic>Female</topic><topic>Humans</topic><topic>Infant</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>Retrospective Studies</topic><topic>Tomography, X-Ray Computed</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hayward, Jean C.</creatorcontrib><creatorcontrib>Titelbaum, David S.</creatorcontrib><creatorcontrib>Clancy, Robert R.</creatorcontrib><creatorcontrib>Zimmerman, Robert A.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of child neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hayward, Jean C.</au><au>Titelbaum, David S.</au><au>Clancy, Robert R.</au><au>Zimmerman, Robert A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Lissencephaly-Pachygyria Associated With Congenital Cytomegalovirus Infection</atitle><jtitle>Journal of child neurology</jtitle><addtitle>J Child Neurol</addtitle><date>1991-04-01</date><risdate>1991</risdate><volume>6</volume><issue>2</issue><spage>109</spage><epage>114</epage><pages>109-114</pages><issn>0883-0738</issn><eissn>1708-8283</eissn><abstract>We report the presence of major cerebral migrational defects in five severely, multiply handicapped children with congenital cytomegalovirus (CMV) infection. 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subjects | Atrophy - pathology Brain - abnormalities Brain - pathology Brain Diseases - complications Brain Diseases - congenital Brain Diseases - diagnosis Brain Diseases - diagnostic imaging Calcinosis - pathology Child Child, Preschool Cytomegalovirus Cytomegalovirus Infections - complications Cytomegalovirus Infections - congenital Female Humans Infant Magnetic Resonance Imaging Male Retrospective Studies Tomography, X-Ray Computed |
title | Lissencephaly-Pachygyria Associated With Congenital Cytomegalovirus Infection |
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