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dc.contributor.author
Siffel, Csaba  
dc.contributor.author
Correa, Adolfo  
dc.contributor.author
Amar, Emmanuelle  
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Bakker, Marian K.  
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Bermejo Sanchez, Eva  
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Bianca, Sebastiano  
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Castilla, Eduardo Enrique  
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Clementi, Maurizio  
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Cocchi, Guido  
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Csaky Szunyogh, Melinda  
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Feldkamp, Marcia L.  
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Landau, Danielle  
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Leoncini, Emanuele  
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Li, Zhu  
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Lowry, R. Brian  
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Marengo, Lisa K.  
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Mastroiacovo, Pierpaolo  
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Morgan, Margery  
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Mutchinick, Osvaldo M.  
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Pierini, Anna  
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Rissmann, Anke  
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Ritvanen, Annukka  
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Scarano, Gioacchino  
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Szabova, Elena  
dc.contributor.author
Olney, Richard S.  
dc.date.available
2023-04-26T13:19:21Z  
dc.date.issued
2011-08  
dc.identifier.citation
Siffel, Csaba; Correa, Adolfo; Amar, Emmanuelle; Bakker, Marian K.; Bermejo Sanchez, Eva; et al.; Bladder Exstrophy: An Epidemiologic Study From the International Clearinghouse for Birth Defects Surveillance and Research, and an Overview of the Literature; Wiley-liss, div John Wiley & Sons Inc.; American Journal Of Medical Genetics Part C-seminars In Medical Genetics; 157; 8-2011; 321-332  
dc.identifier.issn
1552-4868  
dc.identifier.uri
http://hdl.handle.net/11336/195391  
dc.description.abstract
Bladder exstrophy (BE) is a complex congenital anomaly characterized by a defect in the closure of the lower abdominal wall and bladder. We aimed to provide an overview of the literature and conduct an epidemiologic study to describe the prevalence, and maternal and case characteristics of BE. We used data from 22 participating member programs of the International Clearinghouse for Birth Defects Surveillance and Research (ICBDSR). All cases were reviewed and classified as isolated, syndrome, and multiple congenital anomalies. We estimated the total prevalence of BE and calculated the frequency and odds ratios for various maternal and case characteristics. A total of 546 cases with BE were identified among 26,355,094 births. The total prevalence of BE was 2.07 per 100,000 births (95% CI: 1.90–2.25) and varied between 0.52 and 4.63 among surveillance programs participating in the study. BE was nearly twice as common among male as among female cases. The proportion of isolated cases was 71%. Prevalence appeared to increase with increasing categories of maternal age, particularly among isolated cases. The total prevalence of BE showed some variations by geographical region, which is most likely attributable to differences in registration of cases. The higher total prevalence among male cases and older mothers, especially among isolated cases, warrants further attention.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Wiley-liss, div John Wiley & Sons Inc.  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
bladder exstrophy;  
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prevalence;  
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sex ratio;  
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maternal age  
dc.subject.classification
Epidemiología  
dc.subject.classification
Ciencias de la Salud  
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CIENCIAS MÉDICAS Y DE LA SALUD  
dc.title
Bladder Exstrophy: An Epidemiologic Study From the International Clearinghouse for Birth Defects Surveillance and Research, and an Overview of the Literature  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2023-04-05T15:31:48Z  
dc.journal.volume
157  
dc.journal.pagination
321-332  
dc.journal.pais
Estados Unidos  
dc.journal.ciudad
New York  
dc.description.fil
Fil: Siffel, Csaba. National Center on Birth Defects and Developmental Disabilities; Estados Unidos  
dc.description.fil
Fil: Correa, Adolfo. National Center on Birth Defects and Developmental Disabilities; Estados Unidos  
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Fil: Amar, Emmanuelle. Rhone-alps Registry Of Birth Defects Remera; Francia  
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Fil: Bakker, Marian K.. University of Groningen; Países Bajos  
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Fil: Bermejo Sanchez, Eva. Instituto de Salud Carlos III; España  
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Fil: Bianca, Sebastiano. Centro di Consulenza Genetica e di Teratologia della Riproduzione; Italia  
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Fil: Castilla, Eduardo Enrique. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. CEMIC-CONICET. Centro de Educaciones Médicas e Investigaciones Clínicas "Norberto Quirno". CEMIC-CONICET; Argentina. Fundación Oswaldo Cruz; Brasil  
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Fil: Clementi, Maurizio. Università di Padova; Italia  
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Fil: Cocchi, Guido. Bologna University; Italia  
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Fil: Csaky Szunyogh, Melinda. National Center for Healthcare Audit and Inspection; Hungría  
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Fil: Feldkamp, Marcia L.. University of Utah School of Medicine; Estados Unidos  
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Fil: Landau, Danielle. Soroka University Medical Center; Israel  
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Fil: Leoncini, Emanuele. Centre of the International Clearinghouse for Birth Defects Surveillance and Research; Italia  
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Fil: Li, Zhu. Peking University; República de China  
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Fil: Lowry, R. Brian. Alberta Health & Wellness; Canadá  
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Fil: Marengo, Lisa K.. Birth Defects Epidemiology and Surveillance Branch; Estados Unidos  
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Fil: Mastroiacovo, Pierpaolo. Centre of the International Clearinghouse for Birth Defects Surveillance and Research; Italia  
dc.description.fil
Fil: Morgan, Margery. the Congenital Anomaly Register for Wales; Reino Unido  
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Fil: Mutchinick, Osvaldo M.. Instituto Nacional de Ciencias Médicas y Nutrición “Salvador Zubirán”; México  
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Fil: Pierini, Anna. Tuscany Region “Gabriele Monasterio” Foundation; Italia. Consiglio Nazionale delle Ricerche; Italia  
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Fil: Rissmann, Anke. University Magdeburg; Alemania  
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Fil: Ritvanen, Annukka. National Institute for Health and Welfare; Finlandia  
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Fil: Scarano, Gioacchino. General Hospital “G. Rummo” Benevento; Italia  
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Fil: Szabova, Elena. Slovak Medical University; Eslovaquia  
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Fil: Olney, Richard S.. National Center on Birth Defects and Developmental Disabilities; Estados Unidos  
dc.journal.title
American Journal Of Medical Genetics Part C-seminars In Medical Genetics  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/abs/10.1002/ajmg.c.30316  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/https://doi.org/10.1002/ajmg.c.30316