Cytogenetics Additional anomalies First described in a 4-year-old girl with AML M5a with 47,XX,der(7)t(7;10)(p13;p11),+8,der(10)t(7;10)(p13;p 11)t(10;16)(q22;p13),der(16)t(10;16)(q22;p13)/46,XX. Later it was also described in an 84-year-old male without erythrophagocytosis and with this sole cytogenetic aberration. In addition, a variant breakpoint was described in a 52-year-old japanese woman ...
