Skip to main content
Log in

Autosomal dominant macroglossia in two unrelated families

  • Clinical Case Reports
  • Published:
Human Genetics Aims and scope Submit manuscript

Summary

Two unrelated families, one with 15 and the other with 3 members affected with macroglossia as a sole trait, are described. It is concluded that this entity differs from previously reported syndromes presenting macroglossia and is inherited in an autosomal dominant fashion.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Similar content being viewed by others

References

  • Cantú JM, Ruiz C (1985) On atavisms and atavistic genes. Ann Génét (Paris) 28:141–142

    Google Scholar 

  • Martínez y Martínez R, Ocampo-Campos R, Pérez-Arroyo R, Corona-Rivera E, Cantú JM (1985) The Wiedemann-Beckwith syndrome in four sibs including one with associated congenital hypothyroidism. Eur J Pediatr 143:233–235

    Google Scholar 

  • McKusick VA (1983) Mendelian inheritance in man, 6th edn. Johns Hopkins University Press, Baltimore

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Reynoso, M.C., Hernández, A., Soto, F. et al. Autosomal dominant macroglossia in two unrelated families. Hum Genet 74, 200–202 (1986). https://doi.org/10.1007/BF00282095

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00282095

Keywords

Navigation