t ( 10 ; 16 ) ( q 22 ; p 13 )
نویسنده
چکیده
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 with a therapy-related myelodysplastic syndrome (t-MDS) and also this sole translocation. Finally, another fusion variant was described in an AML-M4 female patient with the t(10;16) (q22;p13) and a t(11;17)(q23;q21). Variants There are no cytogenetic variants described, but there are molecular variants due to different breakpoints in the genes fused (see below).
منابع مشابه
inv ( 16 ) ( p 13 q 22 ) , t ( 16 ; 16 ) ( p 13 ; q 22 ) , del ( 16 ) ( q 22 )
inv(16)(p13q22) Gbanding (left) Courtesy Jean-Luc Lai and Alain Vanderhaegen; Rbanding center bottom: Courtesy Christiane Charrin, center top and FISH (top right) -Courtesy Pascale Cornillet-Lefebvre and Stephanie Struski; FISH (bottom right) Courtesy Hossein Mossafa; commercial FISH probes, split in the inv(16). t(16;16)(p13;q22) G-banding Courtesy Diane H. Norback, Eric B. Johnson, and Sara M...
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تاریخ انتشار 2011