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. 2014 Sep 11;9(9):e106906. doi: 10.1371/journal.pone.0106906

Table 2. Clinical characteristics and family history of each patient screened for WFS1 mutations.

No. Family Sex FH ofWFS WFS1mutation DM OA DI D Renal Neuro Psychiatric
1 W1 M Y□ Y 3 4 6
2 W2 F N Y 9 32 32 41 41 + N/A
3 W3 M Y□ Y 6 11 47 19 47
4 W4 M Y□ Y 4 12 12 (Dysarthria, Clumsiness)
5 W5 F N Y 7 10 7 17 20 43 (Brain atrophy, Dizziness) Attempted suicide, Self injury
6 W6a M Y□ Y 5 9 12 12 11 26 (Brain atrophy)
7 W6b M Y□ Y 3 7 19 10 10 24 (Brain atrophy) Depression
8 W6c F Y□ Y 4 6 11 7 7 18 (Brain atrophy) Depression
9 W6d F Y□ Y 5 7 8 5 5 15 (Brain atrophy)
10 W7a M Y□ Y 5 9 4 5 N/A N/A 5(ADHD)
11 W7b M Y□ Y 3 10 3 3 N/A N/A 3(ADHD)
12 W8 M N Y 3 7 5 0
13 W9a M Y□ Y 3 5 + + + 16 (Brain atrophy) Depression
14 W9b M Y□ Y 1.5 5 + + + 16 (Brain atrophy) Depression
15 W9c M Y□ Y 5 + N/A + N/A N/A N/A
16 W10a F Y Y 17 18 N/A Mental retardation
17 W10b F Y Y 10 22 + 38 (Brain atrophy) Depression
18 W11 F N Y 4 9 + 9 +
19 W12 M N Y 27 35 58 42 53 (Brain atrophy)
20 W13 F N Y 13 10
21 W14 F N Y 10 5 29 (Brain atrophy)
22 W15 F N Y 3 + 7 8 7 N/A N/A
23 W16 F N Y 7 18 27 30 (Brain atrophy)
24 W17a F Y□ Y 23 14 + 27 (Brain atrophy, Nystagmus) Mental retardation
25 W17b F Y□ Y 27 <29 25 29 (Brain atrophy, Nystagmus) Mental retardation
26 W17c F Y□ Y 10 <30 + 30 (Brain atrophy, Nystagmus) Mental retardation
27 W18 M Y□ Y 1 <39 39 N/A N/A N/A N/A
28 W19 M N Y§ 3 26
29 W20 F N Y§ 2 14 <41 N/A Mental retardation
30 W21 M N N 30 40 0
31 W22 F N N 11 12 Mental retardation
32 W23 F N N 10 21 <22 (Depression, Self injury)
33 W24 F N N + + N/A + N/A N/A N/A
34 W25 F N N <22 <22 <22 N/A N/A N/A N/A
35 W26 M Y□ N 0(9 M) 7 0(9 M) Spastic paraplegia Mental retardation
36 W27a M Y N 3 <3 <3 Nystagmus Mental retardation
37 W27b M Y N 7 <7 <11
38 W28 F N N 10 <27
39 W29 F N N 10 <29
40 W30 F N N 12 12 +

*M, male; F, female; DM, diabetes mellitus; OA, optic atrophy; D, deafness; DI, diabetes insipidus, numbers indicate age at onset in years; +, symptomatic with unknown onset age; −, asymptomatic, Y; Yes, N; No, N/A; not applicable, □; consanguineous marriage and affected siblings.

§

Individual with detectable WFS1 mutation in single chromosome.