Jackson-Weiss syndrome: Clinical and radiological findings in a large kindred and exclusion of the gene from 7p21 and 5qter

L. C. Ades*, J. C. Mulley, I. P. Senga, L. L. Morris, D. J. David, E. A. Haan

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

22 Citations (Scopus)

Abstract

We describe the clinical and radiological manifestations of the Jackson- Weiss syndrome (JWS) in a large South Australian kindred. Radiological abnormalities not previously described in the hands include coned epiphyses, distal and middle phalangeal hypoplasia, and carpal bone malsegmentation. New radiological findings in the feet include coned epiphyses, hallux valgus, phalangeal, tarso-navicular and calcaneonavicular fusions, and uniform absence of metatarsal fusions. Absence of linkage to eight markers along the short arm of chromosome 7 excluded allelism between JWS and Saethre-Chotzen syndrome at 7p21. No linkage was detected to D5S211, excluding allelism to another recently described cephalosyndactyly syndrome mapping to 5qter.

Original languageEnglish
Pages (from-to)121-130
Number of pages10
JournalAmerican Journal of Medical Genetics
Volume51
Issue number2
DOIs
Publication statusPublished - 1994
Externally publishedYes

Keywords

  • acrocephalosyndactyly
  • autosomal dominant
  • calcaneocuboid fusion
  • craniosynostosis
  • gene mapping
  • Jackson-Weiss syndrome
  • linkage analysis

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