Literature DB >> 22407836

Clinical epidemiology of skeletal dysplasias in South America.

Cecília O Barbosa-Buck1, Iêda M Orioli, Maria da Graça Dutra, Jorge Lopez-Camelo, Eduardo E Castilla, Denise P Cavalcanti.   

Abstract

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: 2.9-3.5). 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: OI-0.74 (0.61-0.89); thanatophoric dysplasia-0.47 (0.36-0.59); and achondroplasia-0.44 (0.33-0.55). 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.
Copyright © 2012 Wiley Periodicals, Inc.

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Year:  2012        PMID: 22407836     DOI: 10.1002/ajmg.a.35246

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  16 in total

Review 1.  Skeletal dysplasias: A radiographic approach and review of common non-lethal skeletal dysplasias.

Authors:  Ananya Panda; Shivanand Gamanagatti; Manisha Jana; Arun Kumar Gupta
Journal:  World J Radiol       Date:  2014-10-28

2.  Novel and Recurrent Mutations in the FGFR3 Gene and Double Heterozygosity Cases in a Cohort of Brazilian Patients with Skeletal Dysplasia.

Authors:  Maria E S Gomes; Thatiane Y Kanazawa; Fernanda R Riba; Natálya G Pereira; Maria C C Zuma; Natana C Rabelo; Maria T Sanseverino; Dafne D G Horovitz; Juan C Llerena; Denise P Cavalcanti; Sayonara Gonzalez
Journal:  Mol Syndromol       Date:  2018-02-02

3.  Application of whole exome sequencing in fetal cases with skeletal abnormalities.

Authors:  Juan Cao; An'er Chen; Liyun Tian; Lulu Yan; Haibo Li; Bihua Zhou
Journal:  Heliyon       Date:  2022-07-06

Review 4.  Achondroplasia: a comprehensive clinical review.

Authors:  Richard M Pauli
Journal:  Orphanet J Rare Dis       Date:  2019-01-03       Impact factor: 4.123

5.  Identification of clinical and radiographic predictors of central nervous system injury in genetic skeletal disorders.

Authors:  Antônio L Cunha; Ana P S Champs; Carla M Mello; Mônica M M Navarro; Frederico J C Godinho; Cássia M B Carvalho; Teresa C A Ferrari
Journal:  Sci Rep       Date:  2021-05-31       Impact factor: 4.379

6.  Skeletal Dysplasias That Cause Thoracic Insufficiency in Neonates: Illustrative Case Reports.

Authors:  Mehmet Sah İpek; Cihan Akgul Ozmen
Journal:  Medicine (Baltimore)       Date:  2016-04       Impact factor: 1.889

7.  Rare diseases: matching wheelchair users with rare metabolic, neuromuscular or neurological disorders to electric powered indoor/outdoor wheelchairs (EPIOCs).

Authors:  Lorraine H De Souza; Andrew O Frank
Journal:  Disabil Rehabil       Date:  2015-12-30       Impact factor: 3.033

8.  Morphology and development of a novel murine skeletal dysplasia.

Authors:  Marta Marchini; Elizabeth Silva Hernandez; Campbell Rolian
Journal:  PeerJ       Date:  2019-07-04       Impact factor: 2.984

9.  Phenotype and genotype analysis of Chinese patients with osteogenesis imperfecta type V.

Authors:  Zeng Zhang; Mei Li; Jin-Wei He; Wen-Zhen Fu; Chang-Qing Zhang; Zhen-Lin Zhang
Journal:  PLoS One       Date:  2013-08-20       Impact factor: 3.240

10.  Genetics and genomics in Brazil: a promising future.

Authors:  Maria Rita Passos-Bueno; Debora Bertola; Dafne Dain Gandelman Horovitz; Victor Evangelista de Faria Ferraz; Luciano Abreu Brito
Journal:  Mol Genet Genomic Med       Date:  2014-07       Impact factor: 2.183

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