Abstract
Unequivocal lymphoblastic leukaemia in a 4-year-old boy was followed 3 years later by equally unequivocal myeloblastic leukaemia in his 20-year-old brother. The boy achieved complete remission and remains well more than 6 years later whereas his brother failed to respond to treatment and died after 5 months. The parents and 3 remaining siblings showed no recognized features suggesting a constitutional predisposition to leukaemia despite thorough investigation.
Full text
PDFPage 271

Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- ANDERSON R. C. Familial leukemia; a report of leukemia in five siblings, with a brief review of the genetic aspects of this disease. AMA Am J Dis Child. 1951 Mar;81(3):313–322. doi: 10.1001/archpedi.1951.02040030323001. [DOI] [PubMed] [Google Scholar]
- Kaur J., Catovsky D., Valdimarsson H., Jensson O., Spiers A. S. Familial acute myeloid leukaemia with acquired Pelger-Huet anomaly and aneuploidy of C group. Br Med J. 1972 Nov 11;4(5836):327–331. doi: 10.1136/bmj.4.5836.327. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kurita S., Kamei Y., Ota K. Genetic studies on familial leukemia. Cancer. 1974 Oct;34(4):1098–1101. doi: 10.1002/1097-0142(197410)34:4<1098::aid-cncr2820340420>3.0.co;2-l. [DOI] [PubMed] [Google Scholar]
- Snyder A. L., Henderson E. S., Li F. P., Todaro G. J. Possible inherited leukaemogenic factors in familial acute myelogenous leukaemia. Lancet. 1970 Mar 21;1(7647):586–589. doi: 10.1016/s0140-6736(70)91626-0. [DOI] [PubMed] [Google Scholar]
