T-cell prolymphocytic leukemia causes: Difference between revisions
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==Causes== | ==Causes== | ||
Common causes of T-cell prolymphocytic leukemia, include genetic factors and chromosomal abnormalities:<ref name="pmid23382603">{{cite journal |vauthors=Graham RL, Cooper B, Krause JR |title=T-cell prolymphocytic leukemia |journal=Proc (Bayl Univ Med Cent) |volume=26 |issue=1 |pages=19–21 |year=2013 |pmid=23382603 |pmc=3523759 |doi= |url=}}</ref> | |||
:*Trisomy 8, chromosomal abnormalities | :*Trisomy 8, chromosomal abnormalities | ||
:*Ataxia telangiectasia (ATM) gene mutation | :*Ataxia telangiectasia (ATM) gene mutation | ||
:*TP53 gene mutation | :*TP53 gene mutation | ||
==References== | ==References== |
Revision as of 18:30, 30 March 2019
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Qurrat-ul-ain Abid, M.D.[2], Maria Fernanda Villarreal, M.D. [3]
Overview
T-cell prolymphocytic leukemia is caused by gene mutations and chromosomal abnormalities. Details of which are described below.
Causes
Common causes of T-cell prolymphocytic leukemia, include genetic factors and chromosomal abnormalities:[1]
- Trisomy 8, chromosomal abnormalities
- Ataxia telangiectasia (ATM) gene mutation
- TP53 gene mutation