Skip to main content

Table 3 Clinical symptoms of XPA patients

From: Genetic investigation of XPA gene: high frequency of the c.682C>T mutation in Moroccan XP patients with moderate clinical profile

Family code

Number of patient/family

Sex

Age

Age of first consultation (m)

Symptoms

Dermatologic

Ocular

Neurologic

XP16

2

F

31

84

++

+

+

F

32

72

++

+

+

XP22

2

M

15

60

++

−

+

  

F

18

18

+

+

++

XP31

1

M

12

36

+

−

+

XP32

2

M

14

72

+

+

+

  

M

16

60

+

+

++

XP39

1

F

33

120

+++

+

+++

XP43

1

M

7

18

+

−

−