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Annals of the Rheumatic Diseases logoLink to Annals of the Rheumatic Diseases
. 1984 Apr;43(2):275–278. doi: 10.1136/ard.43.2.275

A family with multiple musculoskeletal abnormalities.

K E Barber, P J Gow, K M Mayo
PMCID: PMC1001482  PMID: 6424589

Abstract

A family with multiple musculoskeletal abnormalities is reported. The disorder is characterised by platyspondyly, abnormality of the upper femoral epiphyses, and the development of precocious osteoarthritis. It is proposed that this family represents an example of autosomal dominantly inherited spondyloepiphyseal dysplasia tarda (SED tarda).

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Selected References

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

  1. Diamond L. S. A family study of spondyloepiphyseal dysplasia. J Bone Joint Surg Am. 1970 Dec;52(8):1587–1594. [PubMed] [Google Scholar]
  2. MAROTEAUX P., LAMY M., BERNARD J. La dysplasie spondylo-epiphysaire tardive; description clinique et radiologique. Presse Med. 1957 Jun 26;65(51):1205–1208. [PubMed] [Google Scholar]
  3. MacDessi J. J., Kozlowski K., Posen S. Spondylo-epiphyseal dysplasia with ocular changes: report of two "new" variants in two different families. Pediatr Radiol. 1978 Dec 4;7(4):220–228. doi: 10.1007/BF02386712. [DOI] [PubMed] [Google Scholar]
  4. Spranger J., Langer L. O. Spondyloepiphyseal dysplasia. Birth Defects Orig Artic Ser. 1974;10(9):19–61. [PubMed] [Google Scholar]

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