Table 1 of
Ando, Mol Vis 2007;
13:1038-1044.
Table 1. Information on retinitis pigmentosa patients with a family history
Of 68 unrelated RP patients who visited the low-vision clinic at our center, 26 had a family history. Sex: Male (M), Female (F). Siblings and affected siblings include the proband. NB indicates night blindness. Inheritance type: ad indicates autosomal dominant; ar indicates autosomal recessive.
Number
Number of
Patient of affected Type of
Number ID Sex siblings siblings Other affected relatives inheritance
------- ------- ----- -------- -------- ---------------------------- -------------
1 RP005 F 6 2 Mother(RP) ad
2 RP008 F 7 2
3 RP009 F 4 2 Grandmother(NB) ad(?)
4 RP010 F 4 3
5 RP016 F 8 3 Grandmother(RP?) ad(?)
6 RP017 F 5 2
7 RP020 F 3 1 Cousin(central vision loss) ad(?)
8 RP021 M 3 2
9 RP022 M 3 1 Grandfather(RP?) ad(?)
10 RP023 M 7 2
11 RP024 M 2 2 Grandmother(RP?) ad(?)
12 RP029 M 3 2 Mother(NB), cousin(RP) ad
13 RP034 F 5 1 Father(NB), cousin(RP?) ad
14 RP035 M 3 1 Father(RP) ad
15 RP036 F 8 5 Distant relative(RP?) ad(?)
16 RP037 F 3 1 Mother(RP) ad
17 RP038 F 4 1 Cousin(RP) ad(?)
18 RP039 M 2 2
19 RP044 F 6 2
20 RP045 M 10 4
21 RP048 M 4 3 Affected sib's son(RP) ad
22 RP051 F 2 2 Consanguineous marriage ar
23 RP061 M 4 2
24 RP062 M 4 2 Consanguineous marriage ar
25 RP063 M 6 3
26 RP064 F 7 3
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