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SOD-A and chromosome 21

Conflicting findings in a familial translocation (9p24;21q214)

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Summary

A balanced maternal chromosome translocation (9p24;21q214) resulted in two offspring with unbalanced karyotypes. One of these, a girl trisomic for both segment 9pter→9p24 and segment 21pter→21q214, was found to have a SOD-A activity not significantly different from those found in a group of five cases with trisomy 21. However, clinical evaluation of this girl revealed no symptoms of the Down syndrome. These findings suggest that, providing the gene dosage theory is correct, the gene for SOD-A is probably localized on chromosome 21 proximal to, or in, band q21.

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References

  • Feaster WW, Kwok LW, Epstein ChJ (1977) Dosage effects for superoxide dismutase-1 in nucleated cells aneuploid for chromosome 21. Am J Hum Genet 29:563–570

    Google Scholar 

  • Frants RR, Eriksson AW, Jongbloet PH, Hamers AJ (1975) Superoxide dismutase in Down syndrome. Lancet II:42–43

    Google Scholar 

  • Hagemeijer A, Smit EME (1977) Partial trisomy 21. Further evidence that trisomy of band 21q22 is essential for Down's phenotype. Hum Genet 38:15–23

    Google Scholar 

  • Jackson JF, North III ER, Thomas JG (1976) Clinical diagnosis of Down's syndrome. Clin Genet 9:483–487

    Google Scholar 

  • Joenje H, Frants RR, Arwert F, de Bruin GJM, Kostense PJ, van de Kamp JJP, de Koning J, Eriksson AW (1979) Erythrocyte superoxide dismutase deficiency in Fanconi's anemia established by two independent methods of assay. Scand J Clin Lab Invest 39:759–764

    Google Scholar 

  • Kedziora J, Bartosz G, Leyko W, Rozynkowa D (1979) Dismutase activity in translocation trisomy. Lancet I:105

    Google Scholar 

  • Lewandowski RC, Yunis JJ, Lehrke R, O'Leary J, Swaiman KF, Sanchez O (1976) Trisomy for the distal half of the short arm of chromsome 9. A variant of the trisomy 9p syndrome. Am J Dis Child 130:663–667

    Google Scholar 

  • Niebuhr E (1974) Down's syndrome. The possibility of a pathogenetic segment on chromosome no. 21. Humangenetik 21:99–101

    Google Scholar 

  • Philip T, Fraisse J, Sinet PM, Lauras B, Robert JM, Freycon F (1978) Confirmation of the assignment of the human SODs gene to chromosome 21q22. Cytogenet Cell Genet 22:521–523

    Google Scholar 

  • Poisonnier M, Saint-Paul B, Dutrillaux B, Chassaigne M, Gruyer P, de Blignières-Strouk G (1976) Trisome 21 partielle (21q21→ 21q22.2). Ann Genet (Paris) 19:69–73

    Google Scholar 

  • Sinet P-M, Couturier J, Dutrillaux B, Poissonnier M, Raoul O, Rethoré M-O, Allard D, Lejeune J, Jerome H (1976) Trisomie 21 et superoxyde dismutase-1 (IPO-A). Tentative de localisation sur la sous bande 21q22.1. Exp Cell Res 97:47–55

    Google Scholar 

  • Winterbourn CC, Hawkins RE, Brian M, Carrel RW (1975) The estimation of red cell superoxide dismutase activity. J Lab Clin Med 85: 337–341

    Google Scholar 

  • Yamamoto Y, Ogasawara N, Gotoh A, Komiya H, Nakai H, Kuroki Y (1979) A case of 21q-syndrome with normal SOD-1 activity. Hum Genet 48:321–327

    Google Scholar 

  • Yunis JJ, Sawyer JR, Ball DW (1978) The characterization of highresolution G-banded chromosomes of man. Chromosoma 67:293–307

    Google Scholar 

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Leschot, N.J., Slater, R.M., Joenje, H. et al. SOD-A and chromosome 21. Hum Genet 57, 220–223 (1981). https://doi.org/10.1007/BF00282029

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  • DOI: https://doi.org/10.1007/BF00282029

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