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Assessment of fetal intracranial pathologies first demonstrated late in pregnancy: cell proliferation disorders

A considerable number of central nervous system pathologies remain undiagnosed during the first two trimesters of pregnancy. This group of disorders includes anomalies of brain proliferation, migration and cortical organization. Due to the fact that a detailed ultrasound examination of the fetal bra...

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Autores principales: Malinger, Gustavo, Lev, Dorit, Lerman-Sagie, Tally
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC293423/
https://www.ncbi.nlm.nih.gov/pubmed/14617366
http://dx.doi.org/10.1186/1477-7827-1-110
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author Malinger, Gustavo
Lev, Dorit
Lerman-Sagie, Tally
author_facet Malinger, Gustavo
Lev, Dorit
Lerman-Sagie, Tally
author_sort Malinger, Gustavo
collection PubMed
description A considerable number of central nervous system pathologies remain undiagnosed during the first two trimesters of pregnancy. This group of disorders includes anomalies of brain proliferation, migration and cortical organization. Due to the fact that a detailed ultrasound examination of the fetal brain is usually not performed during the third trimester the diagnosis of these disorders is usually only made in families with a previously affected child or in many cases be mere chance. In this article we review the feasibility of prenatal diagnosis of disorders of brain proliferation: microcephaly, macrocephaly, hemimegalencephaly and neoplastic and non-neoplastic abnormal cell types. We discuss the differential diagnosis and offer a stepwise approach to the diagnosis of the more common disorders.
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spelling pubmed-2934232003-12-16 Assessment of fetal intracranial pathologies first demonstrated late in pregnancy: cell proliferation disorders Malinger, Gustavo Lev, Dorit Lerman-Sagie, Tally Reprod Biol Endocrinol Review A considerable number of central nervous system pathologies remain undiagnosed during the first two trimesters of pregnancy. This group of disorders includes anomalies of brain proliferation, migration and cortical organization. Due to the fact that a detailed ultrasound examination of the fetal brain is usually not performed during the third trimester the diagnosis of these disorders is usually only made in families with a previously affected child or in many cases be mere chance. In this article we review the feasibility of prenatal diagnosis of disorders of brain proliferation: microcephaly, macrocephaly, hemimegalencephaly and neoplastic and non-neoplastic abnormal cell types. We discuss the differential diagnosis and offer a stepwise approach to the diagnosis of the more common disorders. BioMed Central 2003-11-14 /pmc/articles/PMC293423/ /pubmed/14617366 http://dx.doi.org/10.1186/1477-7827-1-110 Text en Copyright © 2003 Malinger et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.
spellingShingle Review
Malinger, Gustavo
Lev, Dorit
Lerman-Sagie, Tally
Assessment of fetal intracranial pathologies first demonstrated late in pregnancy: cell proliferation disorders
title Assessment of fetal intracranial pathologies first demonstrated late in pregnancy: cell proliferation disorders
title_full Assessment of fetal intracranial pathologies first demonstrated late in pregnancy: cell proliferation disorders
title_fullStr Assessment of fetal intracranial pathologies first demonstrated late in pregnancy: cell proliferation disorders
title_full_unstemmed Assessment of fetal intracranial pathologies first demonstrated late in pregnancy: cell proliferation disorders
title_short Assessment of fetal intracranial pathologies first demonstrated late in pregnancy: cell proliferation disorders
title_sort assessment of fetal intracranial pathologies first demonstrated late in pregnancy: cell proliferation disorders
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC293423/
https://www.ncbi.nlm.nih.gov/pubmed/14617366
http://dx.doi.org/10.1186/1477-7827-1-110
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