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Su di un Caso con Cariotipo XYY Emopatia Mediterranea ed Ipogammaglobulinemia*

Published online by Cambridge University Press:  01 August 2014

N. Tannoia ,
G. Guanti ,
D. Trizio ,
P. Barsanti  and
L. Bonomo
N. Tannoia*
Affiliation:
Università di Bari Istituto di Clinica Medica Generate e Terapia Istituto di Genetica della Facoltà di Scienze II Cattedra di Clinica Medica
G. Guanti
Affiliation:
Università di Bari Istituto di Clinica Medica Generate e Terapia Istituto di Genetica della Facoltà di Scienze II Cattedra di Clinica Medica
D. Trizio
Affiliation:
Università di Bari Istituto di Clinica Medica Generate e Terapia Istituto di Genetica della Facoltà di Scienze II Cattedra di Clinica Medica
P. Barsanti
Affiliation:
Università di Bari Istituto di Clinica Medica Generate e Terapia Istituto di Genetica della Facoltà di Scienze II Cattedra di Clinica Medica
L. Bonomo
Affiliation:
Università di Bari Istituto di Clinica Medica Generate e Terapia Istituto di Genetica della Facoltà di Scienze II Cattedra di Clinica Medica
*
Istituto di Clinica Medica Generale e Terapia dell'Università di Bari, Italy

Summary

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The case of a 13-year-old boy with Mediterranean disease, hypogammaglobulinemia and XYY sex-chromosome constitution is presented. The somatic cells contained 47 chromosomes. No chromosomal abnormalities were found in the parents and in the brother. The findings are discussed in relation to the previously reported cases of XYY males.

Type
Research Article
Information
Acta geneticae medicae et gemellologiae: twin research , Volume 19 , Issue 3 , July 1970 , pp. 431 - 438
Copyright
Copyright © The International Society for Twin Studies 1970

Footnotes

*

Lavoro eseguito con un contributo CNR (Istituto di Genetica dell'Università di Bari).

References

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