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Original Article

Waardenburg syndrome: A variant with neurological involvement

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Pages 165-170 | Accepted 03 Jul 1987, Published online: 08 Jul 2009

References

  • Arias S. Genetic heterogeneity in the Waardenburg syndrome. Birth Def. 1971; 7: 87–101
  • Cammermeyer J. Refsum's syndrome. Systemic Disorders and Atrophies (Handbook of Clinical Neurology, P. J. Vinken, G. W. Bruyn. North-Holland Publ. Co., Amsterdam 1975; 116–196
  • Goodman R. H., Lewithal I., Solomon A., Klein D. Upper limb involvement in the Klein-Waardenburg syndrome. Amer. J. med. Genet. 1983; 11: 425–433
  • Gorlin R. J., Pindborg J. J., Cohen M. M. Waardenburg syndrome. Syndromes of the Head and Neck, 2nd edn. McGraw-Hill, New York 1976; 709–712
  • Hageman M. J., Delleman J. W. Heterogeneity in Waardenburg syndrome. Amer. J. med. Genet. 1977; 29: 468–485
  • Klein D. Albinisme partiel (leucisme) avec surdi-mudite, blepharophimosis et dysplasie myo-osteo-articulaire. Helv. paediat. Acta 1950; 5: 38–58
  • Klein D. Historical background and evidence for dominant inheritance of the Klein-Waardenburg syndrome (type III). Amer. J. med. Genet. 1983; 14: 231–239
  • Kuroda T., Kitao Y., Yoshida S., Kanzaki Y., Miyamura K., Habu K., Ishikawa T. Two cases of Waardenburg's syndrome without dystopia canthorum (in Japanese). Jibirinshouihou 1983; 76: 175–181
  • McKusick V. A. Congenital deafness and Hirschsprung's disease. New Eng. J. Med. 1973; 288: 691
  • McKusick V. A. Mendelian Inheritance in Man. Catalogs of Autosomal Dominant, Autosomal Recessive, and X-linked Phenotypes, Vllth edn. The Johns Hopkins University Press, Baltimore 1986; 442–443
  • Telfer M. A., Sugar M., Jaeger E. A., Mulcahy J. Dominant piebald trait (white forelock and leukoderma) with neurological impairment. Amer. J. hum. Genet. 1971; 23: 383–389
  • Waardenburg P. J. A new syndrome combining developmental anomalies of the eyelids, eyebrows and nose root with pigmentary defects of the iris and head hair and with congenital deafness. Amer. J. hum. Genet. 1951; 3: 195–253
  • Wilbrandt H. R., Amman F. Nouvelle observation de la forme grave du syndrome de Klein-Waardenburg. Arch. Julius Klaus Stift. Vererb. Forsch. 1964; 39: 80–92

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