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Table 1 Clinical features of 26 males with Kallmann syndrome

From: Clinical and inheritance profiles of Kallmann syndrome in Jordan

FAMILY

No

Age

Anosmia/hyposmia

Synkinesia

Hearing Impairment

Renal abnormalities

Azoospermia

cryptorchidism

Micropenis

1

1

46

+/H

-

+

-

+

+

-

 

2

14

+

+

+

+

+

+

-

 

3

27

+

+

-

+

+

+

-

 

4

20

+

+

-

+

+

+

-

 

5

20

+

+

-

+

+

+

-

 

6

19

+

+

-

+

+

+

-

 

7

16

+

+

-

+

+

+

-

 

8

14

+

+

-

+

NA

+

-

 

9

9

+

+

-

+

NA

+

+

 

10

6

+

+

-

-

NA

-

+

 

11

4

+

+

-

-

NA

+

+

II

1

37

+

-

-

-

+

+

+

 

2

24

+

-

ND*

ND*

ND*

+

+

 

3

22

+

-

ND*

ND*

ND*

-

+

 

4

20

+

-

ND*

ND*

ND*

+

+

III

1

14

+

+

-

-

NA

-

+

 

2

10

+

+

-

+

NA

-

+

 

3

8

+

+

-

+

NA

-

+

IV

1

6

+

+

-

-

NA

+

+

 

2

5

+

+

-

-

NA

+

+

V

1

20

+/H

-

+

-

+

-

+

 

2

19

+/H

+

+

+

+

-

+

VI

1

19

+

-

-

+

ND

+

-

VII

1

37

+

-

-

-

+

+

+

VIII

1

22

+

-

-

+

+

+

+

IX

1

20

+

-

-

-

oligospermia

+

+

  1. NA: not applicable.
  2. ND: not done.
  3. *: lost contact
  4. H: hyposmia