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Dermatoglyphic Analysis in a Highly Mutilating Syndrome*

Published online by Cambridge University Press:  01 August 2014

E. A. Chautard  and
N. Freire-Maia
E. A. Chautard*
Affiliation:
Laboratório de Genética Humana, Universidade Federal do Paraná, Curitiba
N. Freire-Maia
Affiliation:
Laboratório de Genética Humana, Universidade Federal do Paraná, Curitiba
*
Laboratório de Genética Humana, Universidade Federal do Paraná, Caixa Postal 756, Curitiba, Paraná, Brasil

Summary

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This note describes the dermatoglyphic disturbances verified in two patients with a very complex and highly mutilating syndrome. The parents of the affected individuals present, however, normal dermatoglyphics.

Type
Research Article
Information
Acta geneticae medicae et gemellologiae: twin research , Volume 19 , Issue 3 , July 1970 , pp. 421 - 424
Copyright
Copyright © The International Society for Twin Studies 1970

Footnotes

*

Research project sponsored by the National Research Council (Brazil), the Rockefeller Foundation, the Calouste Gulbenkian Foundation, the Research Council of the Federal University of Paraná, and WHO.

References

Freire-Maia, N. (1970). A newly recognized genetic syndrome of tetramelic deficiencies, ectodermal dysplasia, deformed ears, and other abnormalities. Amer. J. Human Genet. (In press).Google Scholar
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Freire-Maia, N., Schetino, M. C., Der Bedrossian, A. A. (1969). Dados clinicos e radiologicos sôbre um sindrome aparentemente nôvo. Ciêna Cult., 21: 280.Google Scholar
Toledo, S. P. A., Saldanha, S. G., Laurenti, R., Saldanha, P. H. (1969). Dermatoglifos digitais e palmares de indíviduos normais da população de Sao Paulo. Rev. Paul. Med., 75: 1.Google Scholar