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 |