Table 3.

Cases with abnormal cytogenetics (n = 14)

CaseKaryotype
46,XX, t(1;13)(q42;q14)[19]/46,XX[1] 
47,XX,+mar[13]/48,idem,+21[7] 
47,XY,+8[13]/46,XY[7] 
46,XY,der(1)t(1;2)(p34;q1?3)[5]/45,idem,10[10]/46,XY[5] 
47,XY,+4[3]/46,XY[17] 
46,XY,del(3)(q21),add(9)(p22)[2]/46,XY[18] 
48,XX,+4,+8[17]/46,XX[3] 
47,XX,+4[19]/46,XX[1] 
46,XY,-6,+r[cp17]/46,XY[3] 
10 47,XY,+8[7]/48,idem,+5[2]/46,XY[cp11] 
11 46,XX,i(21)(q10)[6]/46,XX,idem,?inv(20)(p11.2q12)[6]/46,XX[8] 
12 46,XY,t(3;18)(q26;q21),del(6)(q13q26)[18]/46,XY[2] 
13 46,XX,del(9)(q12q22)[20] 
14 47,XX,+8 [20] 
CaseKaryotype
46,XX, t(1;13)(q42;q14)[19]/46,XX[1] 
47,XX,+mar[13]/48,idem,+21[7] 
47,XY,+8[13]/46,XY[7] 
46,XY,der(1)t(1;2)(p34;q1?3)[5]/45,idem,10[10]/46,XY[5] 
47,XY,+4[3]/46,XY[17] 
46,XY,del(3)(q21),add(9)(p22)[2]/46,XY[18] 
48,XX,+4,+8[17]/46,XX[3] 
47,XX,+4[19]/46,XX[1] 
46,XY,-6,+r[cp17]/46,XY[3] 
10 47,XY,+8[7]/48,idem,+5[2]/46,XY[cp11] 
11 46,XX,i(21)(q10)[6]/46,XX,idem,?inv(20)(p11.2q12)[6]/46,XX[8] 
12 46,XY,t(3;18)(q26;q21),del(6)(q13q26)[18]/46,XY[2] 
13 46,XX,del(9)(q12q22)[20] 
14 47,XX,+8 [20] 

or Create an Account

Close Modal
Close Modal