Bloom's syndrome. V. Surveillance for cancer in affected families
- 1 September 1977
- journal article
- research article
- Published by Wiley in Clinical Genetics
- Vol. 12 (3) , 162-168
- https://doi.org/10.1111/j.1399-0004.1977.tb00919.x
Abstract
The Bloom's Syndrome Registry comprises the 71 individuals in whom this rare genetic disorder has been recognized between the time it was described in 1954 and the end of 1976. The major objective of the Registry is surveillance for cancer in both affected homozygotes and heterozygotes. Of the 61 homozygotes known to have had Bloom's syndrome before cancer was diagnosed and for whom follow‐up has been possible, one in nine has developed cancer. Thirteen cancers have been diagnosed, in 12 individuals. The mean age in 1976 of the living individuals with the syndrome was 16.4 years. The mean age at the time cancer was diagnosed was 20 years. Cancers have been of multiple types and have affected various sites.This publication has 9 references indexed in Scilit:
- Abnormal immune responses of Bloom's syndrome lymphocytes in vitro.Journal of Clinical Investigation, 1975
- A Manyfold Increase in Sister Chromatid Exchanges in Bloom's Syndrome LymphocytesProceedings of the National Academy of Sciences, 1974
- Bloom's syndrome. III. Analysis of the chromosome aberration characteristic of this disorderChromosoma, 1974
- In vitro chromosomal radiosensitivity in “chromosomal breakage syndromes”Cancer, 1973
- Beitrag zum Bloom-SyndromHuman Genetics, 1972
- Genetic Diseases, Chromosome Rearrangements, and MalignancyAnnals of Internal Medicine, 1966
- The syndrome of congenital telangiectaticerythema and stunted growthThe Journal of Pediatrics, 1966
- Chromosomal Breakage in a Rare and Probably Genetically Determined Syndrome of ManScience, 1965
- Cytological Evidence for Crossing-Over in vitro in Human Lymphoid CellsScience, 1964