Multibranched chromosomes 1, 9, and 16 in a patient with combined IgA and IgE deficiency

L. Tiepolo, Paola Maraschio, G. Gimelli, Cristina Cuoco, G. F. Gargani, C. Romano

Research output: Contribution to journalArticle

Abstract

Instability of the centromeric region of chromosome 1 and multibranched configurations formed by different numbers and combinations of arms of chromosomes 1, 9, and 16 were found in cultured lymphocytes of 12-year-old male with combined IgA and IgE deficiency. No chromosome abnormalities were found in fibroblast cultures from the patient or in blood cultures from his parents. A possible effect on the frequency of the abnormalities of the almost continuous antibiotic treatment received by the patient was found both in vivo and in vitro, but no abnormalities were found in blood cultures from control subjects who received similar treatment. Interphase association of chromosomes 1, 9, and 16 and a high frequency of interchanges among the centromeric regions of these chromosomes due to the presence of a fragile site is assumed to be the cause of the abnormalities.

Original languageEnglish
Pages (from-to)127-137
Number of pages11
JournalHuman Genetics
Volume51
Issue number2
DOIs
Publication statusPublished - Oct 1979

ASJC Scopus subject areas

  • Genetics(clinical)
  • Genetics

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    Tiepolo, L., Maraschio, P., Gimelli, G., Cuoco, C., Gargani, G. F., & Romano, C. (1979). Multibranched chromosomes 1, 9, and 16 in a patient with combined IgA and IgE deficiency. Human Genetics, 51(2), 127-137. https://doi.org/10.1007/BF00287166