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GORDON, Hymie

1926–1995
  • Peter Beighton
  • Greta Beighton

Abstract

GORDON syndrome is an autosomal dominant disorder comprising camptodactyly, club foot and cleft palate.

Keywords

Club Foot Cleft Palate Autosomal Dominant Pattern Arthrogryposis Multiplex Congenita Distal Arthrogryposis 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

References

  1. Gordon H, Davies D, Berman MM (1969) Camptodactyly, cleft palate and club foot: a syndrome showing the autosomal dominant pattern of inheritance. J Med Genet 6: 266–274PubMedCrossRefGoogle Scholar
  2. Halal F, Fraser FC (1979) Camptodactyly, cleft palate and club foot (the Gordon syndrome): a report of a large pedigree. J Med Genet 16:149–150PubMedCrossRefGoogle Scholar
  3. Hall JG, Reed SD, Greene G (1982) The distal arthrogryposes: delineation of new entities - review and nosologic discussion. Am J Med Genet 11:185–239PubMedCrossRefGoogle Scholar
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  5. Krieger I, Espiritu CE (1972) Arthrogryposis multiplex congenita and the Turner phenotype. Am J Dis Child 123: 141–144PubMedGoogle Scholar
  6. Moldenhauer E (1964) Zur Klinik des Nielson-Syndroms. Derm Wschr 150: 594–601PubMedGoogle Scholar
  7. Obituary (1995) Cape Times, 7 February p. 7Google Scholar
  8. Obituary (1995) S Afr Med J 85(8): 800–801Google Scholar

Copyright information

© Springer-Verlag New York Limited 1997

Authors and Affiliations

  • Peter Beighton
    • 1
  • Greta Beighton
    • 1
  1. 1.Department of Human GeneticsUniversity of Cape Town Medical SchoolSouth Africa

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