dc.creatorBermejo-Sánchez, Eva
dc.creatorCuevas, Lourdes
dc.creatorAmar, Emmanuelle
dc.creatorBianca, Sebastiano
dc.creatorBianchi, Fabrizio
dc.creatorBotto, Lorenzo D.
dc.creatorCanfield, Mark A.
dc.creatorCastilla, Eduardo E.
dc.creatorClementi, Maurizio
dc.creatorCocchi, Guido
dc.creatorLandau, Danielle
dc.creatorLeoncini, Emanuele
dc.creatorLi, Zhu
dc.creatorLowry, R. Brian
dc.creatorMastroiacovo, Pierpaolo
dc.creatorMutchinick, Osvaldo M.
dc.creatorRissmann, Anke
dc.creatorRitvanen, Annukka
dc.creatorScarano, Gioacchino
dc.creatorSiffel, Csaba
dc.creatorSzabova, Elena
dc.creatorMartínez-Frías, María Luisa
dc.date2017-01-04T18:22:59Z
dc.date2017-01-04T18:22:59Z
dc.date2011
dc.date.accessioned2023-09-26T21:43:30Z
dc.date.available2023-09-26T21:43:30Z
dc.identifierBERMEJO-SÁNCHEZ, Eva; et al. Phocomelia: A Worldwide Descriptive Epidemiologic Study in a Large Series of Cases From the International Clearinghouse for Birth Defects Surveillance and Research, and Overview of the Literature.Am J Med Genet C Semin Med Genet, v.0, n.4, p.305–320, Nov. 2011.
dc.identifier1552-4868
dc.identifierhttps://www.arca.fiocruz.br/handle/icict/16717
dc.identifier10.1002/ajmg.c.30320
dc.identifier1552-4876
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/8873375
dc.descriptionEpidemiologic data on phocomelia are scarce. This study presents an epidemiologic analysis of the largest series of phocomelia cases known to date. Data were provided by 19 birth defect surveillance programs, all members of the International Clearinghouse for Birth Defects Surveillance and Research. Depending on the program, data corresponded to a period from 1968 through 2006. A total of 22,740,933 live births, stillbirths and, for some programs, elective terminations of pregnancy for fetal anomaly (ETOPFA) were monitored. After a detailed review of clinical data, only true phocomelia cases were included. Descriptive data are presented and additional analyses compared isolated cases with those with multiple congenital anomalies (MCA), excluding syndromes. We also briefly compared congenital anomalies associated with nonsyndromic phocomelia with those presented with amelia, another rare severe congenital limb defect. A total of 141 phocomelia cases registered gave an overall total prevalence of 0.62 per 100,000 births (95% confidence interval: 0.52-0.73). Three programs (Australia Victoria, South America ECLAMC, Italy North East) had significantly different prevalence estimates. Most cases (53.2%) had isolated phocomelia, while 9.9% had syndromes. Most nonsyndromic cases were monomelic (55.9%), with an excess of left (64.9%) and upper limb (64.9%) involvement. Most nonsyndromic cases (66.9%) were live births; most isolated cases (57.9%) weighed more than 2,499 g; most MCA (60.7%) weighed less than 2,500 g, and were more likely stillbirths (30.8%) or ETOPFA (15.4%) than isolated cases. The most common associated defects were musculoskeletal, cardiac, and intestinal. Epidemiological differences between phocomelia and amelia highlighted possible differences in their causes.
dc.description2030-01-01
dc.formatapplication/pdf
dc.languageeng
dc.publisherWiley
dc.rightsrestricted access
dc.subjectEpidemiologia
dc.subjectPrevalência
dc.subjectEctromelia
dc.subjectFrequência
dc.subjectphocomelia
dc.subjectepidemiology
dc.subjectprevalence
dc.subjectfrequency
dc.subjectICBDSR
dc.titlePhocomelia: a worldwide descriptive epidemiologic study in a large series of cases from the International Clearinghouse for Birth Defects Surveillance and Research, and overview of the literature
dc.typeArticle


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