Spontaneous cytogenetic abnormalities in lymphocytes from thirteen patients with ataxia telangiectasia
โ Scribed by A. M. R. Taylor; J. M. Oxford; J. A. Metcalfe
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- French
- Weight
- 676 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0020-7136
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โฆ Synopsis
Abstract
Ataxia telangiectasia (AT) is a human autosomal recessive disorder in which patients show a marked predisposition to malignant disease and cytogenetic abnormalities. We report here the levels of spontaneously occurring chromosome aberrations and particularly the presence of cytogenetically marked clones of cells in peripheral lymphocytes of 13 patients. There is a variation between the patients with respect to frequency of different aberration types, and clones are present in 5/13 patients. Several of these patients appear to have more than a single clone, possible clones or subclones. There is no evidence for any malignant disease in any of these patients. A description is given from one of these patients, of the most complex clone so far reported in an AT patient without malignant disease. The development of such a complex clone might be important as a step in malignant change. Similarities between this clone and one reported in an AT patient with Tโcell chronic lymphocytic leukaemia are discussed.
๐ SIMILAR VOLUMES
Ataxia telangiectasia (A-T) is an autosomal recessive disorder in which patients show an unusual predisposition to malignant disease, including T-cell chronic lymphocytic leukaemia. We report here the steady growth over 5 years of a complex, cytogenetically abnormal clone of T lymphocytes in an A-T
Previously, we have reported significantly lower immunoglobulin (lg) A production in supernatants of cultured lymphoblastoid cells using enzyme-linked immunosorbent assay from patients with ataxia-telangiectasia (AT) when compared to that of age-and sexmatched healthy individuals. Here, we further a
Cytogenetic analysis of a cemento-ossifying fibroma from a patient with nonfamilial bilateral multicentric retinoblastoma revealed three reciprocal translocations with the karyotype 46,XY,t( I; I8)(q2 I ;q2 I .3),t(3; I O)(p I3;q22).t(6; I I)(p22;p 15). Routine and high-resolution cytogenetic analys
Ataxia telangiectasia (A-T) is an autosomal recessive disorder in which patients show an unusual predisposition to lymphoid malignancies including T-cell leukaemia. We compare here the surface phenotypes of fresh and cultured A-T T cells. A total of 17 T-cell cultures from 8 A-T patients are compare