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Malays J Pathol ; 38(3): 311-313, 2016 Dec.
Article in English | MEDLINE | ID: mdl-28028302

ABSTRACT

Acute promyelocytic leukaemia (APML) is characterised by the t(15;17)(q22;q21), that results in the fusion of the promyelocytic leukaemia (PML) gene at 15q22 with the retinoic acid α-receptor (RARA) gene at 17q21. The current case report describes a 13-year-old male with APML, who was negative for PML/RARA fusion signal but reported to have an atypical translocation t(16;17). To the best of our knowledge this is the first case report of APML responsive to ATRA with such a translocation.


Subject(s)
Chromosomes, Human, Pair 16/genetics , Chromosomes, Human, Pair 17/genetics , Leukemia, Promyelocytic, Acute/genetics , Adolescent , Humans , Karyotyping , Male , Real-Time Polymerase Chain Reaction , Translocation, Genetic
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