AUTHOREA
Log in Sign Up Browse Preprints

loading page

Rare chromosomal translocations associated with pediatric case of AML cup like: t(4;12)(q12; p13), t(1;16)(q12;q24) and t(12;13)(p13;q13)
  • +4
  • Hamdaoui Hasna,
  • Abdelhafid Natiq,
  • Oumaima Benlarroubia,
  • Faiza CHBEL,
  • Rajaa Chahboun,
  • jihane Toughza,
  • Afaf Lamzouri
Hamdaoui Hasna
University Hospital Center, Tangier-Tetouan-Alhoceima

Corresponding Author:[email protected]

Author Profile
Abdelhafid Natiq
faculty of medecine and pharmacy, Mohammed V University
Author Profile
Oumaima Benlarroubia
Mohammed VI University of Health Sciences
Author Profile
Faiza CHBEL
Ecole Normale supérieure , Casablanca
Author Profile
Rajaa Chahboun
Universite Abdelmalek Essaadi Faculte de Medecine et de Pharmacie - Tanger
Author Profile
jihane Toughza
Mohammed VI University of Health Sciences Faculty of Medicine
Author Profile
Afaf Lamzouri
Université Abdelmalek Essaadi Faculté de Médecine et de Pharmacie - Tanger
Author Profile

Abstract

Cup Like acute myeloid leukemia is the rarest form of children leukemia. We present a case of Cup Like Acute Myeloid Leukemia (AML) with t(4;12) (q12;p13) associated with two other clones t(1;16)(q12;q24) and t(12;13)(p13;q13). Cytogenetic and iFISH are highly relevant for the prognosis of and therapeutic decisions in LAM.

Peer review status:IN REVISION

19 Oct 2022Submitted to Clinical Case Reports
Show details
Hide details
24 Oct 2022Submission Checks Completed
24 Oct 2022Assigned to Editor
04 Dec 2022Reviewer(s) Assigned
09 Dec 2022Review(s) Completed, Editorial Evaluation Pending
23 Mar 2023Editorial Decision: Revise Minor