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Table 3 Summary of reported Xp22; Yq11 and Xp22; Yp11 translocation

From: Comprehensive analysis of three female patients with different types of X/Y translocations and literature review

The exception type

 

Type I

Type II

Type III

Type IV

Type V

 

Gender

M

F

M

F

M

F

M

F

M

F

Category

Number

33

0

2

53

2

2

7

2

6

0

Origin

Pat

0

0

0

1

0

0

0

0

0

0

Mat

29

0

0

8

0

0

0

0

0

0

De novo

0

0

1

8

1

0

2

1

2

0

Unknown

4

0

1

36

1

2

5

1

4

0

Stature

Short

26

0

0

42

2

1

4

0

2

0

Normal

6

0

2

10

0

0

3

1

0

0

Unknown

1

0

0

1

0

1

0

1

4

0

Limbs

Short

12

0

0

8

0

0

2

1

4

0

Normal

21

0

2

45

2

2

5

1

2

0

Unknown

0

0

0

0

0

0

0

0

0

0

Gonad

Abnormal

10

0

1

9

2

1

3

0

3

0

Normal

1

0

0

27

0

0

1

1

0

0

Unknown

22

0

1

17

0

1

3

1

3

0

Psychomotor movements

Abnormal

10

0

0

4

0

0

0

0

3

0

Normal

22

0

2

49

2

2

7

1

3

0

Unknown

1

0

0

0

0

0

0

1

0

0

Mental

Abnormal

13

0

0

4

0

0

0

0

2

0

Normal

17

0

2

47

2

2

7

1

4

0

Unknown

3

0

0

2

0

0

0

1

0

0

Facial deformities

P

15

0

1

7

0

0

1

0

3

0

Eye abnormalities

P

1

0

0

2

0

0

0

1

0

0

Ichthyosis

P

12

0

0

1

0

0

1

0

0

0

Chondrodysplasia punctata

P

6

0

0

1

0

0

1

0

0

0

Leri-Weill dyschondrosteosis

P

9

0

0

4

0

1

1

0

2

0

  1. M male, F female, P positive, patients present with this clinical phenotype, Pat paternal, Mat maternal. Unknown: There is no mention of the relevant circumstances in the text