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Germ line mutations associated with leukemias

Porter, Christopher C.·2016·Hematology
DOI 10.1182/asheducation-2016.1.302
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Abstract

Several genetic syndromes have long been associated with a predisposition to the development of leukemia, including bone marrow failure syndromes, Down syndrome, and Li Fraumeni syndrome. Recent work has better defined the leukemia risk and outcomes in these syndromes. Also, in the last several years, a number of other germ line mutations have been discovered to define new leukemia predisposition syndromes, including ANKRD26, GATA2, PAX5, ETV6, and DDX41. In addition, data suggest that a substantial proportion of patients with therapy related leukemias harbor germ line mutations in DNA damage response genes such as BRCA1/2 and TP53. Recognition of clinical associations, acquisition of a thorough family history, and high index-of-suspicion are critical in the diagnosis of these leukemia predisposition syndromes. Accurate identification of patients with germ line mutations associated with leukemia can have important clinical implications as it relates to management of the leukemia, as well as genetic counseling of family members.

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Metadata

Authors
Porter, C. C.
Venue
Hematology
Publisher
American Society of Hematology
Published
2016-12-02
Volume
2016
Issue
1
Pages
302-308
ISSN
  • 1520-4391
  • 1520-4383
DOI
10.1182/asheducation-2016.1.302
Cited by
51
References
3
Language
en

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CoChat. (2026). Citation check: Germ line mutations associated with leukemias. https://app.cochat.ai/papers/10.1182/asheducation-2016.1.302
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Porter, C. C. (2016). Germ line mutations associated with leukemias. Hematology. https://doi.org/10.1182/asheducation-2016.1.302