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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Clinical epidemiology of skeletal dysplasias in South America

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Autor(es):
Barbosa-Buck, Cecilia O. [1] ; Orioli, Ieda M. [2, 3] ; Dutra, Maria da Graca [2, 4] ; Lopez-Camelo, Jorge [2, 5] ; Castilla, Eduardo E. [2, 4, 5] ; Cavalcanti, Denise P. [1]
Número total de Autores: 6
Afiliação do(s) autor(es):
[1] Univ Estadual Campinas UNICAMP, Dept Med Genet, Fac Ciencias Med, Sao Paulo - Brazil
[2] INAGEMP, Rio De Janeiro - Brazil
[3] Univ Fed Rio de Janeiro, ECLAMC, Dept Genet, Inst Biol, Rio De Janeiro - Brazil
[4] Inst Oswaldo Cruz, Lab Epidemiol Malformacoes Congenitas, ECLAMC, Sao Paulo - Brazil
[5] CEMIC, ECLAMC, Buenos Aires, DF - Argentina
Número total de Afiliações: 5
Tipo de documento: Artigo Científico
Fonte: AMERICAN JOURNAL OF MEDICAL GENETICS PART A; v. 158A, n. 5, p. 1038-1045, MAY 2012.
Citações Web of Science: 22
Resumo

Currently accepted birth prevalence for osteochondrodysplasias (OCD) of about 2/10,000 is based on few studies from small series of cases. We conducted a study based on more than 1.5 million births. OCD cases were detected from 1,544,496 births occurring and examined in 132 hospitals of ECLAMC (Latin American Collaborative Study of Congenital Malformations) between 2000 and 2007. Cases were detected and registered according to a pre-established protocol, and then ranked in four diagnostic evidence levels (DEL), according to available documentation. For the analysis of risk factors, a healthy control sample born in the same period was used. OCD was diagnosed in 492 newborns, resulting in a prevalence per 10,000 of 3.2 (95% CI: 2.93.5). Perinatal lethality (stillbirths plus early neonatal deaths) occurred in 50% of cases. Prenatal ultrasound diagnosis was made in 73% of cases (n=359). Among 211 cases from the best documented group (DEL-1) and according to international classification, 33% of cases fit into the G-25 (osteogenesis imperfecta), 29% in Group-1 (FGFR3), and 8% in Group-18 (Bent bones). The prevalence of the main OCD types were: OI0.74 (0.610.89); thanatophoric dysplasia0.47 (0.360.59); and achondroplasia0.44 (0.330.55). Paternal age (31.2 +/- 8.5), parity (2.6), and parental consanguinity rate (5.4%) were higher in cases than in controls (P<0.001). In conclusion, the OCD overall prevalence of 3.2 per 10,000 found seems to be more realistic than previous estimates. This study also confirmed the high perinatal mortality, and the association with high paternal age, parity, and parental consanguinity rate. (c) 2012 Wiley Periodicals, Inc. (AU)

Processo FAPESP: 98/16006-6 - Estudo da etiopatogenia dos defeitos congênitos de alta morbi-mortalidade no período perinatal
Beneficiário:Denise Pontes Cavalcanti
Modalidade de apoio: Auxílio à Pesquisa - Regular