Spondyloepiphyseal dysplasia tarda: Report of a family with autosomal dominant transmission

Authors

  • Kim Schantz
  • Poul Erik Andersen
  • Per Justesen

DOI:

https://doi.org/10.3109/17453678809149433

Abstract

We present a clinical and radiographic study of a family with the autosomal dominant form of spondyloepiphyseal dysplasia tarda, in some patients associated with hearing deficiency. Although no causal treatment is possible, correct diagnosis is important to avoid unnecessary treatment and for information about prognosis, genetic counseling, and recommendation of future occupation.

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Published

1988-01-01

How to Cite

Schantz, K., Andersen, P. E., & Justesen, P. (1988). Spondyloepiphyseal dysplasia tarda: Report of a family with autosomal dominant transmission. Acta Orthopaedica, 59(6), 716–719. https://doi.org/10.3109/17453678809149433

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