Skip to main content
Log in

A new lethal skeletal dysplasia or the severe end of the atelosteogenesis spectrum?

  • Published:
Pediatric Radiology Aims and scope Submit manuscript

Abstract

The case of a 20-week fetus is reported with almost completely deficient ossification of the vertebral bodies and absent ossification of several long bones. This could be a unique skeletal dysplasia or the most severe end of the atelosteogenesis spectrum.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Maroteaux P, Spranger J, Stanescu V, et al (1982) Atelosteogenesis. Am J Med Genet 13: 15–25

    Google Scholar 

  2. Temple K, Hall CA, Chitty L, Baraitser M (1990) A case of atelosteogenesis.J Med Genet 27:194–197

    Google Scholar 

  3. Herzberg AJ, Effmann EL, Bradford WD (1988) Variant of atelosteogenesis? Report of a 20-week fetus. Am J Med Genet 29:883–890

    Google Scholar 

  4. Kozlowski K, Sillence D, Cortis-Jones R, Osborn R (1985) Boomerang dysplasia. Br J Radiol 58:369–371

    Google Scholar 

  5. Hunter AGW, Carpenter BF (1991) Atelosteogenesis 1 and boomerang dysplasia: a question of nosology. Clin Genet 39:471–480

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Fryer, A.E., Carty, H. A new lethal skeletal dysplasia or the severe end of the atelosteogenesis spectrum?. Pediatr Radiol 26, 678–679 (1996). https://doi.org/10.1007/BF01356834

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01356834

Keywords

Navigation