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Journal of Medical Genetics logoLink to Journal of Medical Genetics
. 1996 May;33(5):429–431. doi: 10.1136/jmg.33.5.429

A new case of fibrochondrogenesis from Spain.

M L Martínez-Frías 1, A García 1, J Cuevas 1, J I Rodríguez 1, M Urioste 1
PMCID: PMC1050618  PMID: 8733059

Abstract

A rare, neonatally lethal chondrodysplasia with histological characteristics was first described in 1978 and the authors named the condition fibrochondrogenesis. Here we report the eighth published case of fibrochondrogenesis. This was identified in a population of 1,158,067 consecutive livebirths, so we can assume that this figure should be the minimal prevalence for livebirths.

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Selected References

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

  1. Eteson D. J., Adomian G. E., Ornoy A., Koide T., Sugiura Y., Calabro A., Lungarotti S., Mastroiacovo P., Lachman R. S., Rimoin D. L. Fibrochondrogenesis: radiologic and histologic studies. Am J Med Genet. 1984 Oct;19(2):277–290. doi: 10.1002/ajmg.1320190210. [DOI] [PubMed] [Google Scholar]
  2. Lazzaroni-Fossati F., Stanescu V., Stanescu R., Serra G., Magliano P., Maroteaux P. La fibrochondrogénèse. Arch Fr Pediatr. 1978 Dec;35(10):1096–1104. [PubMed] [Google Scholar]
  3. Whitley C. B., Langer L. O., Jr, Ophoven J., Gilbert E. F., Gonzalez C. H., Mammel M., Coleman M., Rosemberg S., Rodriques C. J., Sibley R. Fibrochondrogenesis: lethal, autosomal recessive chondrodysplasia with distinctive cartilage histopathology. Am J Med Genet. 1984 Oct;19(2):265–275. doi: 10.1002/ajmg.1320190209. [DOI] [PubMed] [Google Scholar]

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