Table I.
Translocation | De novo/hereditary | Author, study | Abnormality | (Refs.) |
---|---|---|---|---|
45,XY,-22,der(15),t(15;22)(q26.2;q11.2) | De novo | Present case | VCFS | |
45,XX,-3,-22, +der(3),t(3;22)(p25;q11) | De novo/IVF | Faed et al, 1987 | DGS | (15) |
46,XY,-15,+der(22),t(15;22)(q13;q11) | Paternal | Van Hove et al, 1992 | DGS + duplication of 22q11 | (12) |
46,XY,t(15;22)(q22;q13) | De novo | Fryns, 1993 | DGS | (13) |
45,XX,der(4)t(4;22)(p16.3;q11.2),-22 | Maternal | Reddy et al, 1996 | DGS + Wolf-Hirschhorn deletions | (16) |
46,XX,der(15),t(15;22)(p11.2;q11.2),-22 | De novo | Jaquez et al, 1997 | DGS + VCGS | (11) |
t(9;22)(q34.3;q11.2) | Paternal | McGoey et al, 2009 | DGS + 9q subtelomeric deletion | (19) |
45,XY,der(3)t(3;22)(p25;q11),-22 | De novo | Dundar et al, 2010 | VCFS + 3p deletion | (17) |
45,XX,der(6)t(6;22)(p25.3;q11.21),-22 | De novo/FIV | Gollo Dantas et al, 2016 | DGS | (10) |
46,XX,r(22); | De novo | Kashevarova, et al, 2018 | 22q13.32-q13.33 deletion | (20) |
IVF, in vitro fertilization; VCFS, Velo-cardio-facial syndrome; DGS, DiGeorge syndrome; t, translocation; r, ring chromosome.