Skip to main content
Journal of Medical Genetics logoLink to Journal of Medical Genetics
. 1986 Aug;23(4):328–332. doi: 10.1136/jmg.23.4.328

The birth prevalence rates for the skeletal dysplasias.

I M Orioli, E E Castilla, J G Barbosa-Neto
PMCID: PMC1049699  PMID: 3746832

Abstract

This study was undertaken to establish the prevalence rates at birth of the skeletal dysplasias that can be recognised in the perinatal period. Using the data base of the Latin-American Collaborative Study of Congenital Malformations (ECLAMC), for the years 1978 to 1983, on 349 470 births (live and stillbirths), a crude prevalence rate of 2.3/10 000 was observed. However, several indications of under-registration suggest that the real value is about twice that observed. The most frequent types of skeletal dysplasia were achondroplasia, with a prevalence rate between 0.5 and 1.5/10 000 births, the thanatophoric dysplasia/achondrogenesis group (0.2 and 0.5/10 000 births), and osteogenesis imperfecta (0.4/10 000 births). The mutation rate for autosomal dominant achondroplasia was estimated at between 1.72 and 5.57 X 10(-5) per gamete per generation.

Full text

PDF
328

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Byers P. H., Bonadio J. F., Steinmann B. Osteogenesis imperfecta: update and perspective. Am J Med Genet. 1984 Feb;17(2):429–435. doi: 10.1002/ajmg.1320170206. [DOI] [PubMed] [Google Scholar]
  2. Curran J. P., Sigmon B. A., Opitz J. M. Lethal forms of chondrodysplastic dwarfism. Pediatrics. 1974 Jan;53(1):76–85. [PubMed] [Google Scholar]
  3. Gustavson K. H., Jorulf H. Different types of osteochondrodysplasia in a consecutive series of newborns. Helv Paediatr Acta. 1975 Oct;30(3):307–314. [PubMed] [Google Scholar]
  4. Maroteaux P., Cohen-Solal L. L'ostéogenèse imparfaite létale. Définition, hétérogénéité. Ann Genet. 1984;27(1):11–15. [PubMed] [Google Scholar]
  5. Orioli I. M., Castilla E. E., Carvalho W. P. Inbreeding in a South-American newborn series. Acta Anthropogenet. 1982;6(1):45–55. [PubMed] [Google Scholar]

Articles from Journal of Medical Genetics are provided here courtesy of BMJ Publishing Group

RESOURCES