Table 1 of
Iqbal, Mol Vis 2020; 26:334-344.
Table 1. Clinical characteristics of families PKCC193, PKCC202, and PKCC220 harboring mutations in FYCO1.
| Family ID | Individual ID | Sex | Age at first symptoms * | Age at enrollment | Visual Acuity (OD/OS) | Clinical Findings |
|---|---|---|---|---|---|---|
| PKCC193 | 11 | F | 2.5 months | 7 years | PL/PL | B/L cataracts, B/L nystagmus |
| 12 | F | 4 months | 1 year | PL/PL | B/L cataracts, squint | |
| 16 | M | 11 months | 32 years | CF/CF | B/L cataracts | |
| 17 | M | 1.5 years | 36 years | CF/CF | B/L cataracts, B/L nystagmus | |
| PKCC202 | 10 | M | 4 months | 10 months | CF/CF | B/L cataracts |
| 11 | F | 3 months | 6.5 years | No PL/CF | B/L cataracts | |
| PKCC220 | 7 | F | 5 months | 4 years | CF/CF | B/L cataracts |
| 8 | F | 3 months | 9 months | CF/CF | B/L cataracts |