scholarly journals Complex karyotype with cryptic FUS gene rearrangement and deletion of NR3C1 and VPREB1 genes in childhood B‑cell acute lymphoblastic leukemia: A case report

Author(s):  
Moneeb Othman ◽  
Marina Đurišić ◽  
Gordana Samardzija ◽  
Dragana Vujić ◽  
Nina Lakic ◽  
...  
2011 ◽  
Vol 5 (1) ◽  
Author(s):  
Muhammad N Siddique ◽  
Muhammad Popalzai ◽  
Nelly Aoun ◽  
Rabih Maroun ◽  
Michael Awasum ◽  
...  

2021 ◽  
pp. 1031-1039
Author(s):  
Ahmed Arafat ◽  
Dinara Sadykova ◽  
Ayrat Ziatdinov ◽  
Svetlana Senek ◽  
Natalya Samoilova ◽  
...  

SARS-CoV-2 which causes COVID-19 has been a great challenge to treat and deal with; despite strict measures that had been implemented by governments and organizations, worrying rates of morbidity and mortality are still being reported. Although available data have expressed that moderate or even mild forms of the disease are expected amongst most pediatrics cases, minimal data are available on the prognosis and the disease’s complications on the immunocompromised, especially oncology patients. We report a case of relapsed precursor B-cell acute lymphoblastic leukemia of a child with Down syndrome and COVID-19 and outline the treatment regimen that we used.


2016 ◽  
Vol 1 (2) ◽  
pp. 132-138 ◽  
Author(s):  
Karen A. Dun ◽  
Rob Vanhaeften ◽  
Tracey J. Batt ◽  
Louise A. Riley ◽  
Giuseppe Diano ◽  
...  

Key Points BCR-ABL1 rearrangement as a subclonal change in ETV6-RUNX1–positive B-ALL is a rare occurrence not previously reported. The prognosis of this rare subclonal change has not been determined, yet inclusion of tyrosine kinase inhibitors in treatment is ubiquitous.


2016 ◽  
Vol 11 (3) ◽  
pp. 2117-2122 ◽  
Author(s):  
MONEEB A.K. OTHMAN ◽  
BEATA GRYGALEWICZ ◽  
BARBARA PIENKOWSKA-GRELA ◽  
JOLANTA RYGIER ◽  
ANNA EJDUK ◽  
...  

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