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Costituzione Cromosomica 46, XX in Ermafrodita Umano Ambigonadico

Published online by Cambridge University Press:  01 August 2014

V. Tomašić ,
J. Sepčić ,
M. Kružić ,
P. Ledić ,
S. Ćuk  and
K. Juranić
V. Tomašić*
Affiliation:
Facoltà di Medicina di Rijeka, Università di Zagabria Istituto di Biologia Generale Clinica Malattie Nervose e Mentali
J. Sepčić
Affiliation:
Facoltà di Medicina di Rijeka, Università di Zagabria Istituto di Biologia Generale Clinica Malattie Nervose e Mentali
M. Kružić
Affiliation:
Facoltà di Medicina di Rijeka, Università di Zagabria Istituto di Biologia Generale Clinica Malattie Nervose e Mentali
P. Ledić
Affiliation:
Facoltà di Medicina di Rijeka, Università di Zagabria Istituto di Biologia Generale Clinica Malattie Nervose e Mentali
S. Ćuk
Affiliation:
Facoltà di Medicina di Rijeka, Università di Zagabria Istituto di Biologia Generale Clinica Malattie Nervose e Mentali
K. Juranić
Affiliation:
Facoltà di Medicina di Rijeka, Università di Zagabria Istituto di Biologia Generale Clinica Malattie Nervose e Mentali
*
dipl. biol., Medicinski Facultet, Rijeka, Jugoslavia

Summary

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The authors present the case of a 42 years old hermaphrodite, showing bilateral ambigonadism with female nuclear sex and 46,XX karyotype. The psychological analysis reveals a female personality, which is in contrast with the male civil status: hence, a source of frustration and social inadaptation.

Type
Research Article
Information
Acta geneticae medicae et gemellologiae: twin research , Volume 19 , Issue 3 , July 1970 , pp. 425 - 430
Copyright
Copyright © The International Society for Twin Studies 1970

References

Bibliografia

Atakam, A. M. (1954). A case of hermaphroditismus masculinus internus. Ann. Surg., 140: 216.Google Scholar
Clayton, G. W., O'Heeron, M. K., Smith, J. D., Grabstald, H. (1957). A case of true hermaphrodism: possible relationship to Klinefelter's syndrome. J. Clin. Endrocr., 17: 1002.Google Scholar
Crossfield, J. H. (1962). True hermaphrodism including a case with chromosome analysis. J. Urol., 88: 674.Google Scholar
De Assis, L. M., Epps, D. R., Bottura, C., Ferrari, J. (1960). Chromosomal constitution and nuclear sex of a true hermaphrodite. Lancet, 11: 129.Google Scholar
Ferguson-Smith, M. A., Johnston, A. W., Weinberg, A. N. (1960). The chromosome complement in true hermaphroditism. Lancet, 11: 126.Google Scholar
Ford, C. E. (1962). Human cytogenetics. Acta Genet. Med. Gemellol., 3: 253.Google Scholar
Fraccaro, M., Taylor, A. I., Bodian, M., Newns, G. H. (1962). A human intersex (« true hermaphrodite») with XX/XXY/XXYYY sex chromosomes. Cytogenetics (Basel), 1: 104.Google Scholar
Gordon, R. R., O'Gorman, F. J. F., Dewhurst, C. J., Blank, C. E. (1960). Chromosome count in a hermaphrodite with some features of Klinefelter's syndrome. Lancet, 7153: 736.Google Scholar
Hander, D. G., Armstrong, C. N. (1959). The chromosomes of a true hermaphrodite. Brit. Med. J., 2: 187.Google Scholar
Hungerford, D. A., Donnelly, A. J., Nowell, P. C., Beck, S. (1959). The chromosome constitution of a human phenotypic intersex. Amer. J. Hum. Genet., 11: 215.Google Scholar
Hungerford, D. A., Donnelly, A. J., Nowell, P. C., Beck, S. (1964). The chromosome constitution of a human phenotypic intersex: reconfirmation of a 46 chromosome, XX, apparently non mosaic « true hermaphrodite ». Hereditas (Lund), 52: 379.Google Scholar
Mc Govern, J. H., Marshall, V. E. (1962). Three cases of true hermaphrodism. J. Urol., 88: 680.Google Scholar
Root, A. W., Eberlein, W. R., Briebart, S., Moorhead, P. S., Mellman, W.J. (1964). Chromosomal analysis of multiple tissues from a true hermaphrodite. J. Clin. Endocr., 24: 467.Google Scholar
Rosenberg, H., Clayton, G. W., Hsu, T. C. (1962). Familial true hermaphrodism with a normal female genotype. Proc. X Int. Cong. Pediat., Lisboa.Google Scholar
Sasaki, M. S., Makino, S. (1960). The chromosomal constitution of a human hermaphrodite. Texas Rep. Biol. Med., 18: 493.Google Scholar