Epidemiology of holoprosencephaly: Prevalence and risk factors

Autores
Orioli, Iêda M.; Castilla, Eduardo Enrique
Año de publicación
2010
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
The wide variation in cerebral and facial phenotypes and the recognized etiologic heterogeneity of holoprosencephaly (HPE) contribute to the observed inter-study heterogeneity. High lethality during the early stages of embryonic and fetal development makes HPE detection age dependent. By reviewing 21 HPE epidemiologic articles, the observed prevalence rate differences can be largely explained by the pregnancy outcome status of the studied cohort: livebirth, stillbirth, and terminations of pregnancy (TOPs): lower than 1 per 10,000 when live and still births were included, higher when TOPs were included, and between 40 and 50 per 10,000 in two classical Japanese studies on aborted embryos. The increasing secular trend observed in some studies probably resulted from an increasing use of prenatal sonography. Ethnic variations in birth prevalence rates (BPRs) could occur in HPE, but the available data are not very convincing. Higher BPRs were generally observed in the less favored minorities (Blacks, Hispanics, Pakistanis), suggesting a bias caused by a lower prenatal detection rate of HPE, and consequently less TOPs. Severe ear defects, as well as microstomia, were part of the spectrum of HPE. Non-craniofacial anomalies, more frequently associated with HPE than expected, were genital anomalies (24%), postaxial polydactyly (8%), vertebral defects (5%), limb reduction defects (4%), and transposition of great arteries (4%). The variable female predominance, found in different HPE studies, could also depend on the proportion of early conceptions in each study sample, as males are more likely to be lost through spontaneous abortions. © 2010 Wiley-Liss, Inc.
Fil: Orioli, Iêda M.. Universidade Federal do Rio de Janeiro; Brasil
Fil: Castilla, Eduardo Enrique. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Instituto Oswaldo Cruz; Brasil. Centro de Educación Médica e Investigaciones Clínicas “Norberto Quirno”; Argentina
Materia
Associated Malformations
Ethnicity
Gender
Geographical Variation
Holoprosencephaly
Prevalence
Time Variation
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/53643

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spelling Epidemiology of holoprosencephaly: Prevalence and risk factorsOrioli, Iêda M.Castilla, Eduardo EnriqueAssociated MalformationsEthnicityGenderGeographical VariationHoloprosencephalyPrevalenceTime Variationhttps://purl.org/becyt/ford/3.3https://purl.org/becyt/ford/3The wide variation in cerebral and facial phenotypes and the recognized etiologic heterogeneity of holoprosencephaly (HPE) contribute to the observed inter-study heterogeneity. High lethality during the early stages of embryonic and fetal development makes HPE detection age dependent. By reviewing 21 HPE epidemiologic articles, the observed prevalence rate differences can be largely explained by the pregnancy outcome status of the studied cohort: livebirth, stillbirth, and terminations of pregnancy (TOPs): lower than 1 per 10,000 when live and still births were included, higher when TOPs were included, and between 40 and 50 per 10,000 in two classical Japanese studies on aborted embryos. The increasing secular trend observed in some studies probably resulted from an increasing use of prenatal sonography. Ethnic variations in birth prevalence rates (BPRs) could occur in HPE, but the available data are not very convincing. Higher BPRs were generally observed in the less favored minorities (Blacks, Hispanics, Pakistanis), suggesting a bias caused by a lower prenatal detection rate of HPE, and consequently less TOPs. Severe ear defects, as well as microstomia, were part of the spectrum of HPE. Non-craniofacial anomalies, more frequently associated with HPE than expected, were genital anomalies (24%), postaxial polydactyly (8%), vertebral defects (5%), limb reduction defects (4%), and transposition of great arteries (4%). The variable female predominance, found in different HPE studies, could also depend on the proportion of early conceptions in each study sample, as males are more likely to be lost through spontaneous abortions. © 2010 Wiley-Liss, Inc.Fil: Orioli, Iêda M.. Universidade Federal do Rio de Janeiro; BrasilFil: Castilla, Eduardo Enrique. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Instituto Oswaldo Cruz; Brasil. Centro de Educación Médica e Investigaciones Clínicas “Norberto Quirno”; ArgentinaWiley-liss, Div John Wiley & Sons Inc2010-02info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/53643Orioli, Iêda M.; Castilla, Eduardo Enrique; Epidemiology of holoprosencephaly: Prevalence and risk factors; Wiley-liss, Div John Wiley & Sons Inc; American Journal Of Medical Genetics Part C-seminars In Medical Genetics; 154; 1; 2-2010; 13-211552-4868CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1002/ajmg.c.30233info:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/abs/10.1002/ajmg.c.30233info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-10-15T15:36:39Zoai:ri.conicet.gov.ar:11336/53643instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-10-15 15:36:39.825CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Epidemiology of holoprosencephaly: Prevalence and risk factors
title Epidemiology of holoprosencephaly: Prevalence and risk factors
spellingShingle Epidemiology of holoprosencephaly: Prevalence and risk factors
Orioli, Iêda M.
Associated Malformations
Ethnicity
Gender
Geographical Variation
Holoprosencephaly
Prevalence
Time Variation
title_short Epidemiology of holoprosencephaly: Prevalence and risk factors
title_full Epidemiology of holoprosencephaly: Prevalence and risk factors
title_fullStr Epidemiology of holoprosencephaly: Prevalence and risk factors
title_full_unstemmed Epidemiology of holoprosencephaly: Prevalence and risk factors
title_sort Epidemiology of holoprosencephaly: Prevalence and risk factors
dc.creator.none.fl_str_mv Orioli, Iêda M.
Castilla, Eduardo Enrique
author Orioli, Iêda M.
author_facet Orioli, Iêda M.
Castilla, Eduardo Enrique
author_role author
author2 Castilla, Eduardo Enrique
author2_role author
dc.subject.none.fl_str_mv Associated Malformations
Ethnicity
Gender
Geographical Variation
Holoprosencephaly
Prevalence
Time Variation
topic Associated Malformations
Ethnicity
Gender
Geographical Variation
Holoprosencephaly
Prevalence
Time Variation
purl_subject.fl_str_mv https://purl.org/becyt/ford/3.3
https://purl.org/becyt/ford/3
dc.description.none.fl_txt_mv The wide variation in cerebral and facial phenotypes and the recognized etiologic heterogeneity of holoprosencephaly (HPE) contribute to the observed inter-study heterogeneity. High lethality during the early stages of embryonic and fetal development makes HPE detection age dependent. By reviewing 21 HPE epidemiologic articles, the observed prevalence rate differences can be largely explained by the pregnancy outcome status of the studied cohort: livebirth, stillbirth, and terminations of pregnancy (TOPs): lower than 1 per 10,000 when live and still births were included, higher when TOPs were included, and between 40 and 50 per 10,000 in two classical Japanese studies on aborted embryos. The increasing secular trend observed in some studies probably resulted from an increasing use of prenatal sonography. Ethnic variations in birth prevalence rates (BPRs) could occur in HPE, but the available data are not very convincing. Higher BPRs were generally observed in the less favored minorities (Blacks, Hispanics, Pakistanis), suggesting a bias caused by a lower prenatal detection rate of HPE, and consequently less TOPs. Severe ear defects, as well as microstomia, were part of the spectrum of HPE. Non-craniofacial anomalies, more frequently associated with HPE than expected, were genital anomalies (24%), postaxial polydactyly (8%), vertebral defects (5%), limb reduction defects (4%), and transposition of great arteries (4%). The variable female predominance, found in different HPE studies, could also depend on the proportion of early conceptions in each study sample, as males are more likely to be lost through spontaneous abortions. © 2010 Wiley-Liss, Inc.
Fil: Orioli, Iêda M.. Universidade Federal do Rio de Janeiro; Brasil
Fil: Castilla, Eduardo Enrique. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Instituto Oswaldo Cruz; Brasil. Centro de Educación Médica e Investigaciones Clínicas “Norberto Quirno”; Argentina
description The wide variation in cerebral and facial phenotypes and the recognized etiologic heterogeneity of holoprosencephaly (HPE) contribute to the observed inter-study heterogeneity. High lethality during the early stages of embryonic and fetal development makes HPE detection age dependent. By reviewing 21 HPE epidemiologic articles, the observed prevalence rate differences can be largely explained by the pregnancy outcome status of the studied cohort: livebirth, stillbirth, and terminations of pregnancy (TOPs): lower than 1 per 10,000 when live and still births were included, higher when TOPs were included, and between 40 and 50 per 10,000 in two classical Japanese studies on aborted embryos. The increasing secular trend observed in some studies probably resulted from an increasing use of prenatal sonography. Ethnic variations in birth prevalence rates (BPRs) could occur in HPE, but the available data are not very convincing. Higher BPRs were generally observed in the less favored minorities (Blacks, Hispanics, Pakistanis), suggesting a bias caused by a lower prenatal detection rate of HPE, and consequently less TOPs. Severe ear defects, as well as microstomia, were part of the spectrum of HPE. Non-craniofacial anomalies, more frequently associated with HPE than expected, were genital anomalies (24%), postaxial polydactyly (8%), vertebral defects (5%), limb reduction defects (4%), and transposition of great arteries (4%). The variable female predominance, found in different HPE studies, could also depend on the proportion of early conceptions in each study sample, as males are more likely to be lost through spontaneous abortions. © 2010 Wiley-Liss, Inc.
publishDate 2010
dc.date.none.fl_str_mv 2010-02
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/53643
Orioli, Iêda M.; Castilla, Eduardo Enrique; Epidemiology of holoprosencephaly: Prevalence and risk factors; Wiley-liss, Div John Wiley & Sons Inc; American Journal Of Medical Genetics Part C-seminars In Medical Genetics; 154; 1; 2-2010; 13-21
1552-4868
CONICET Digital
CONICET
url http://hdl.handle.net/11336/53643
identifier_str_mv Orioli, Iêda M.; Castilla, Eduardo Enrique; Epidemiology of holoprosencephaly: Prevalence and risk factors; Wiley-liss, Div John Wiley & Sons Inc; American Journal Of Medical Genetics Part C-seminars In Medical Genetics; 154; 1; 2-2010; 13-21
1552-4868
CONICET Digital
CONICET
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language eng
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dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
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dc.publisher.none.fl_str_mv Wiley-liss, Div John Wiley & Sons Inc
publisher.none.fl_str_mv Wiley-liss, Div John Wiley & Sons Inc
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instname:Consejo Nacional de Investigaciones Científicas y Técnicas
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