Table 1 of
Manayath, Mol Vis 2014; 20:724-731.
Table 1. Genotype of the family members in the study.
Individual ID | Age /Sex | Family member’s relation with the Proband | Disease state | Genotype | Genotype Status |
---|---|---|---|---|---|
1–1 | 40/F | Proband | Affected | GG | Affected homozygote |
1–2 | 41/F | Sister | Normal | AG | Carrier heterozygote |
1–3 | 48/M | Husband | Normal | AA | Normal homozygous |
1–4 | 12/F | Daughter | Normal | AG | Carrier heterozygote |
1–5 | 14/M | Son | Normal | AG | Carrier heterozygote |
1–6 | 75/M | Father | Normal | AG | Carrier heterozygote |
1–7 | 70/F | Mother | Normal | AG | Carrier heterozygote |
1–8 | 42/M | Brother | Similar clinical features of proband | GG | Affected homozygote |
1–9 | 9/F | Brother’s daughter | Normal | AG | Carrier heterozygote |
1–10 | 9/F | Brother’s daughter | Normal | AG | Carrier heterozygote |
1–11 | 16/F | Sister’s daughter | Normal | AA | Normal homozygous |
1–12 | 13/F | Sister’s daughter | Normal | AG | Carrier heterozygote |