Chromosomal abnormalities other than monosomy 7 alone
Karyotype . |
|---|
| 45,XY,-7/45,XY,-7,der(18)?del(18)(q1?) |
| 45,XX,add(2)(q32),-7,add(13)(q32) |
| 45,XY,-7→45,XY,-7,del(12)(p11p12)* |
| 46,XX→47,XX,+21/46,XX,-7,+21* |
| 45,XY,-7→45,XY,-7[28]/45,XY, -7,t(8;14)(q22;q13)[3]* |
| 46,XY,+der(1)t(1;7)(p11;p11), -7→47,XY,+der(1)t(1;7)(p11;p11),-7, +8*† |
| 46,XX→47,XX,+8* |
| 47,XX,?del(2)(pter),+8/48,idem,+21 |
| 47,XX,+8 |
| 47,XX,+8 |
| 47,XY,+8 |
| 47∼48,XX,+?8,+mar[cp6] |
| 48,XY,+X,+8 |
| 46,XY,ins(16;?)(q23;?)[7]/45,XY,ins(16;?)(q23;?),-21[5] |
| 43-45,XX,del(7)/43-44,XX,del(7),del(9),del(14),del(19),del(21) |
| 46,XX,der(10)(q24) |
| 46,XY,t(X;17)(p11.2;q25) |
| 46,XX,del(7)(q11q32) |
| 46,XX,der(1),t(1;7)(p11;p11) |
Karyotype . |
|---|
| 45,XY,-7/45,XY,-7,der(18)?del(18)(q1?) |
| 45,XX,add(2)(q32),-7,add(13)(q32) |
| 45,XY,-7→45,XY,-7,del(12)(p11p12)* |
| 46,XX→47,XX,+21/46,XX,-7,+21* |
| 45,XY,-7→45,XY,-7[28]/45,XY, -7,t(8;14)(q22;q13)[3]* |
| 46,XY,+der(1)t(1;7)(p11;p11), -7→47,XY,+der(1)t(1;7)(p11;p11),-7, +8*† |
| 46,XX→47,XX,+8* |
| 47,XX,?del(2)(pter),+8/48,idem,+21 |
| 47,XX,+8 |
| 47,XX,+8 |
| 47,XY,+8 |
| 47∼48,XX,+?8,+mar[cp6] |
| 48,XY,+X,+8 |
| 46,XY,ins(16;?)(q23;?)[7]/45,XY,ins(16;?)(q23;?),-21[5] |
| 43-45,XX,del(7)/43-44,XX,del(7),del(9),del(14),del(19),del(21) |
| 46,XX,der(10)(q24) |
| 46,XY,t(X;17)(p11.2;q25) |
| 46,XX,del(7)(q11q32) |
| 46,XX,der(1),t(1;7)(p11;p11) |