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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)
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  • 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]

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Abdelhafid Natiq
faculty of medecine and pharmacy, Mohammed V University
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Oumaima Benlarroubia
Mohammed VI University of Health Sciences
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Ecole Normale supérieure , Casablanca
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Rajaa Chahboun
Universite Abdelmalek Essaadi Faculte de Medecine et de Pharmacie - Tanger
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jihane Toughza
Mohammed VI University of Health Sciences Faculty of Medicine
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Afaf Lamzouri
Université Abdelmalek Essaadi Faculté de Médecine et de Pharmacie - Tanger
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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.
19 Oct 2022Submitted to Clinical Case Reports
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