Central nervous system abnormalities on midline facial defects with hypertelorism detected by magnetic resonance image and computed tomography

Detalhes bibliográficos
Autor(a) principal: Gil-da-Silva-Lopes,Vera Lúcia
Data de Publicação: 2006
Outros Autores: Giffoni,Silvio David Araújo
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Arquivos de neuro-psiquiatria (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2006000600005
Resumo: The aim of this study were to describe and to compare structural central nervous system (CNS) anomalies detected by magnetic resonance image (MRI) and computed tomography (CT) in individuals affected by midline facial defects with hypertelorism (MFDH) isolated or associated with multiple congenital anomalies (MCA). The investigation protocol included dysmorphological examination, skull and facial X-rays, brain CT and/or MRI. We studied 24 individuals, 12 of them had an isolated form (Group I) and the others, MCA with unknown etiology (Group II). There was no significative difference between Group I and II and the results are presented in set. In addition to the several CNS anomalies previously described, MRI (n=18) was useful for detection of neuronal migration errors. These data suggested that structural CNS anomalies and MFDH seem to have an intrinsic embryological relationship, which should be taken in account during the clinical follow-up.
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spelling Central nervous system abnormalities on midline facial defects with hypertelorism detected by magnetic resonance image and computed tomographyfrontonasal dysplasiahypertelorismmidlinecraniofacial abnormalitiesfacial cleftsCNS abnormalitiesmagnetic resonance imageThe aim of this study were to describe and to compare structural central nervous system (CNS) anomalies detected by magnetic resonance image (MRI) and computed tomography (CT) in individuals affected by midline facial defects with hypertelorism (MFDH) isolated or associated with multiple congenital anomalies (MCA). The investigation protocol included dysmorphological examination, skull and facial X-rays, brain CT and/or MRI. We studied 24 individuals, 12 of them had an isolated form (Group I) and the others, MCA with unknown etiology (Group II). There was no significative difference between Group I and II and the results are presented in set. In addition to the several CNS anomalies previously described, MRI (n=18) was useful for detection of neuronal migration errors. These data suggested that structural CNS anomalies and MFDH seem to have an intrinsic embryological relationship, which should be taken in account during the clinical follow-up.Academia Brasileira de Neurologia - ABNEURO2006-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2006000600005Arquivos de Neuro-Psiquiatria v.64 n.4 2006reponame:Arquivos de neuro-psiquiatria (Online)instname:Academia Brasileira de Neurologiainstacron:ABNEURO10.1590/S0004-282X2006000600005info:eu-repo/semantics/openAccessGil-da-Silva-Lopes,Vera LúciaGiffoni,Silvio David Araújoeng2006-12-21T00:00:00Zoai:scielo:S0004-282X2006000600005Revistahttp://www.scielo.br/anphttps://old.scielo.br/oai/scielo-oai.php||revista.arquivos@abneuro.org1678-42270004-282Xopendoar:2006-12-21T00:00Arquivos de neuro-psiquiatria (Online) - Academia Brasileira de Neurologiafalse
dc.title.none.fl_str_mv Central nervous system abnormalities on midline facial defects with hypertelorism detected by magnetic resonance image and computed tomography
title Central nervous system abnormalities on midline facial defects with hypertelorism detected by magnetic resonance image and computed tomography
spellingShingle Central nervous system abnormalities on midline facial defects with hypertelorism detected by magnetic resonance image and computed tomography
Gil-da-Silva-Lopes,Vera Lúcia
frontonasal dysplasia
hypertelorism
midline
craniofacial abnormalities
facial clefts
CNS abnormalities
magnetic resonance image
title_short Central nervous system abnormalities on midline facial defects with hypertelorism detected by magnetic resonance image and computed tomography
title_full Central nervous system abnormalities on midline facial defects with hypertelorism detected by magnetic resonance image and computed tomography
title_fullStr Central nervous system abnormalities on midline facial defects with hypertelorism detected by magnetic resonance image and computed tomography
title_full_unstemmed Central nervous system abnormalities on midline facial defects with hypertelorism detected by magnetic resonance image and computed tomography
title_sort Central nervous system abnormalities on midline facial defects with hypertelorism detected by magnetic resonance image and computed tomography
author Gil-da-Silva-Lopes,Vera Lúcia
author_facet Gil-da-Silva-Lopes,Vera Lúcia
Giffoni,Silvio David Araújo
author_role author
author2 Giffoni,Silvio David Araújo
author2_role author
dc.contributor.author.fl_str_mv Gil-da-Silva-Lopes,Vera Lúcia
Giffoni,Silvio David Araújo
dc.subject.por.fl_str_mv frontonasal dysplasia
hypertelorism
midline
craniofacial abnormalities
facial clefts
CNS abnormalities
magnetic resonance image
topic frontonasal dysplasia
hypertelorism
midline
craniofacial abnormalities
facial clefts
CNS abnormalities
magnetic resonance image
description The aim of this study were to describe and to compare structural central nervous system (CNS) anomalies detected by magnetic resonance image (MRI) and computed tomography (CT) in individuals affected by midline facial defects with hypertelorism (MFDH) isolated or associated with multiple congenital anomalies (MCA). The investigation protocol included dysmorphological examination, skull and facial X-rays, brain CT and/or MRI. We studied 24 individuals, 12 of them had an isolated form (Group I) and the others, MCA with unknown etiology (Group II). There was no significative difference between Group I and II and the results are presented in set. In addition to the several CNS anomalies previously described, MRI (n=18) was useful for detection of neuronal migration errors. These data suggested that structural CNS anomalies and MFDH seem to have an intrinsic embryological relationship, which should be taken in account during the clinical follow-up.
publishDate 2006
dc.date.none.fl_str_mv 2006-12-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2006000600005
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2006000600005
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0004-282X2006000600005
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Academia Brasileira de Neurologia - ABNEURO
publisher.none.fl_str_mv Academia Brasileira de Neurologia - ABNEURO
dc.source.none.fl_str_mv Arquivos de Neuro-Psiquiatria v.64 n.4 2006
reponame:Arquivos de neuro-psiquiatria (Online)
instname:Academia Brasileira de Neurologia
instacron:ABNEURO
instname_str Academia Brasileira de Neurologia
instacron_str ABNEURO
institution ABNEURO
reponame_str Arquivos de neuro-psiquiatria (Online)
collection Arquivos de neuro-psiquiatria (Online)
repository.name.fl_str_mv Arquivos de neuro-psiquiatria (Online) - Academia Brasileira de Neurologia
repository.mail.fl_str_mv ||revista.arquivos@abneuro.org
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