Hostname: page-component-cd9895bd7-q99xh Total loading time: 0 Render date: 2024-12-24T20:52:56.109Z Has data issue: false hasContentIssue false
  • English
  • Français

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

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

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

Bibliografia

Akesson, H. O., Forssman, H., Wallin, L. (1968). Chromosome of tall men in mental hospitals. Lancet, 2: 1040.CrossRefGoogle ScholarPubMed
Balodimos, M. C., Lisco, H., Irwin, I., Merrill, W., Dingman, J. F. (1966). XYY karyotype in a case of familial hypogonadism. J. Clin. Endocr., 26: 443–452.Google Scholar
Bartlett, D. J., Hurley, W. P., Brand, C. R., Poole, E. W. (1968). Chromosomes of male patients in a security prison. Nature (London), 219: 351–354.Google Scholar
Boczkowski, K., Casey, M. D. (1967). Pattern of DNA replication of the sex chromosomes in three males, two with XYY and one with XXYY karyotype. Nature (London), 213: 928–930.Google Scholar
Borgaonkar, D. S., Murdoch, I. L., McKusick, V. A., Burkowf, S. P., Money, J. W. (1968). The YY syndrome. Lancet, 2: 461.Google Scholar
Casey, M. D., Blank, C. E., Street, D. R. K., Segall, L. J., McDougall, J. H., McGrath, P. J. (1966). YY chromosome and antisocial behaviour. Lancet, 2: 859–860.Google Scholar
Celermajer, J. M., Bowdler, J. D., Cohen, D. H. (1968). Pulmonary stenosis in patients with the Turner phenotype in the male. Amer. J. Dis. Child., 116: 351–358.Google Scholar
Court Brown, W. N., Harnden, D. G., Jacobs, S. P., MacLean, N., Mantle, D. J. (1964). Abnormalities of the sex chromosome complement in man. Spec. Rep. Ser. Med. Res. Coun. (London), N. 305.Google Scholar
Court Brown, W. N., Price, W. H., Jacobs, S. P. (1968). Further information on the identity of 47, XYY males. Brit. Med. J., 1: 325–328.Google Scholar
Dammacco, F., Bonomo, L. (1967). Agamma e disgammaglobulinemia: aspetti clinici e biologici. Recent. Progr. Med. (Roma), 42: 573–601.Google Scholar
Dent, T., Edwards, J. H., Delhanty, J. D. A. (1963). A partial mongol. Lancet, 2: 484–487.Google Scholar
Emerit, I., De Grouchy, J., Frezal, J., Josso, N., Corone, P., Vernant, P., Soulie, P., Lamy, M. (1968). Caryotype XYY, anomalies cardiovasculaires et dysmorphie faciale chez un garcon de 12 ans. Arch. Franc. Pediat., 25: 531–539.Google Scholar
Forssman, H., Akesson, H. O., Wallin, L. (1968). The YY syndrome. Lancet, 2: 779.Google Scholar
Franks, R. G., Bunting, K. W., Engel, E. (1967). Male pseudohermaphroditism with XYY sex chromosomes. J. Clin. Endocr., 17: 1623–1627.Google Scholar
Gilgenkrantz, S., Beurey, J., Weber, M., Gurecki, H. (1968). Le syndrome YY. A propos de deux observations XYY et XXYY. Ann. Med. Nancy, 7: 26–37.Google Scholar
Goodman, R. M., Smith, W. S., Migeon, C. J., (1967). Sex chromosome abnormalities. Nature (London), 216: 942–943.Google Scholar
Griffiths, A. W., Zaremba, J. (1967). Crime and sex chromosome anomalies. Brit. Med. J., 4: 622.Google Scholar
Gustavson, K. H., Verneholt, J. (1968). The XYY syndrome in a prepuberal boy. Hereditas (Lund), 60: 264–266.Google Scholar
Hauschka, T. S., Hasson, J. E., Goldstein, M. N., Koepf, G. F., Sandberg, A. A. (1962). An XYY man with progeny indicating familial tendency to non-disjunction. Amer. J. Hum. Genet., 14: 22–30.Google Scholar
Hustinx, T. W. J., van Olphen, A. H. F. (1963). An XYY chromosome pattern in a boy with Marfan's syndrome. Genetica, 34: 262–269.Google Scholar
Ismail, A. A. A., Harkness, A. A., Kirkham, K. E., Loraine, J. A., Whatmore, P. B., Brittain, R. P. (1968). Effect of abnormal sex-chromosome complements on urinary testosterone levels. Lancet, 1: 220–222.CrossRefGoogle Scholar
Jacobs, P. A., Brunton, M., Melville, M. M. (1965). Aggressive behaviour, mental sub-normality and the XYY male. Nature (London), 208: 1351–1352.Google Scholar
Jacobs, P. A., Price, W. H., Court Brown, W. M. (1968). Chromosome studies on men in a Maximum Security Hospital. Ann. Hum. Genet., 31: 339–358.Google Scholar
Kosenow, W., Pfeiffer, R. A. (1966). YY syndrome with multiple malformations. Lancet, 1: 1375–1376.Google Scholar
Kosenow, W., Pfeiffer, R. A. (1967). YY Syndrom. Mschr. Kinderheilk, 115: 24–31.Google Scholar
Leff, J. P., Scott, P. D. (1968). XYY and intelligence. Lancet, 1: 645.Google Scholar
Mancini, G., Carbonara, A. O., Heremans, Y. F. (1965). Immunochemical quantitation of antigens by single radial immunodiffusion. Immunochemistry, 2: 235.CrossRefGoogle ScholarPubMed
Mintzer, R., Pergament, E., Berlow, S., Sato, H. J. (1968). The XYY syndrome. J. Pediat., 72: 572.Google Scholar
Mirouze, J., Emberger, J. M., Jaffiol, C., Orsetti, A., Meynadier, J. (1966). Hypopubérisme simple et luxation bilatérale des coudes avec aberration chromosomique (présence d'un petit acrocentrique supplémentaire). Sem. Hop. Paris, 42: 753–756.Google Scholar
Montero, E., Duran, I. (1965). XYY gonosomic polysomy. An. Desarrollo, 13: 215–222.Google Scholar
Nielsen, J., Christensen, A. L., Johnsen, S. G., Frøland, A. (1966). Psychopathology and testis histology in a patient with the XYY syndrome. Acta Med. Scand., 180: 747–757.Google Scholar
Nielsen, J., Christensen, A. L., Johnsen, S. G., Frøland, A. (1968 a). The XYY syndrome in a mental hospital. Brit. J. Criminol., 186–203.Google Scholar
Nielsen, J., Tsuboi, T., Sturup, G., Romano, D. (1968 b). XYY chromosomal constitution in criminal psychopaths. Lancet, 2: 576.Google Scholar
Pergament, E., Sato, H., Berlow, S., Mintzer, R. (1968). YY syndrome in an American Negro. Lancet, 2: 281.CrossRefGoogle Scholar
Papanicolaou, A. D., Kirkham, K. E., Loraine, J. A., (1968). Abnormalities in urinary gonadotrophin excretion in men with a 47, XYY sex chromosome constitution. Lancet, 2: 608–610.Google Scholar
Persson, T. (1967). An XYY man and his relatives. J. Ment. Defic. Res., 11: 239–245.Google ScholarPubMed
Price, W. H., Strong, J. A., Whatmore, P. B., McClemont, W. F. (1966). Criminal patients with XYY sex chromosome complement. Lancet, 1: 565–566.Google Scholar
Price, W. H., Whatmore, P. B. (1967 a). Criminal behaviour and the XYY male. Nature (London), 213: 815–816.Google Scholar
Price, W. H., Whatmore, P. B. (1967 b). Behaviour disorders and pattern of crime among XYY males identified at a Maximum Security Hospital. Brit. Med. J., 1: 533–536.Google Scholar
Price, W. H., Whatmore, P. B. (1968). The electrocardiogram in males with extra Y chromosomes. Lancet, 1: 1106–1108.Google Scholar
Ricci, N., Malacarne, P. (1964). An XYY human male. Lancet, 1: 721.Google Scholar
Richards, B. W., Stewart, A. (1966). The YY syndrome. Lancet, 1: 984–985.CrossRefGoogle Scholar
Rudd, B. T., Galal, O. M., Casey, M. D. (1968). Testosterone excretion rates in normal males and males with an XYY complement. J. Med. Genet., 5: 286–288.Google Scholar
Sandberg, A. A., Koepf, G. F., Ishihara, T., Hauschka, T. S. (1961). XYY human male. Lancet, 2: 488.Google Scholar
Telfer, A. M., Baker, D., Longtin, L. (1968 a). YY syndrome in an American Negro. Lancet, 1: 95.Google Scholar
Telfer, A. M., Baker, D., Clark, G. R., Richardson, C. E. (1968 b). Incidence of gross chromosomal errors among tall criminal American males. Science, 159: 1249–1250.Google Scholar
Thompson, H. (1967). J. Med. Genet., 5: 341–359. Cit. Court Brown et al, 1968.Google Scholar
Thompson, H., Melnyk, J., Hecht, F. (1967). Reproduction and meiosis in XYY. Lancet, 2: 831.Google Scholar
Thorburn, M. J., Chutkan, W., Richards, R., Bell, R. (1968). XYY sex chromosomes in a Jamaican with orthopaedic abnormalities. J. Med. Genet., 5: 215–219.CrossRefGoogle Scholar
Turner, B., Jennings, A. N. (1961). Trisomy for chromosome 22. Lancet, 2: 49.Google Scholar
Tzoneva-Maneva, M. T., Bosajieva, E., Petrov, B. (1966). Chromosomal abnormalities in idiopathic osteoarthropathy. Lancet, 1: 1000–1002.Google Scholar
Uchida, I. A., Miller, J. R., Soltan, H. C. (1964). Dermatoglyphics associated with the XXYY chromosome complement. Amer. J. Hum. Genet., 16: 284–291.Google Scholar
Valentine, G. H., Sergovich, F. (1967). A new dilemma. Lancet, 2: 151.Google Scholar
Vignetti, P., Capotorti, L., Ferrante, E. (1964). XYY chromosomal constitution with genital abnormality. Lancet, 1: 588–589.Google Scholar
Vignetti, P., Capotorti, L., Ferrante, E. (1965). Su di un caso di pseudoermafroditismo maschile a 47 cromosomi. Minerva Pediat., 17: 596–597.Google Scholar
Wiener, S., Sutherland, G. (1968). A normal XYY man. Lancet, 2: [1352.Google Scholar
Wiener, S., Sutherland, G., Bartholomew, A. A., Hudson, B. (1968). XYY males in a Melbourne prison. Lancet, 1: 150.CrossRefGoogle Scholar
Wilton, E., Lever, A. (1966). The YY syndrome. Lancet, 1: 1156.Google Scholar