Table 2.
Descriptive statistics for the demographics, genetic characterization, and follow-up time of the retinitis pigmentosa patients.
| N (%) | Age During Visit 1 (yr) | Age During Visit 2 (yr) | |||||
|---|---|---|---|---|---|---|---|
| Patients | 22 | 36.03 ± 16.69 | 38.26 ± 16.71 | ||||
| Males | 13 (59.1) | ||||||
| Females | 9 (40.9) | ||||||
| Disease subtype | Disease-causing Gene Variants (# of patients) | ||||||
| ARRP | 8 (36.3) | CDHR1 (1), DHDDS (1), MAK (1), Unknown (5) | |||||
| ADRP | 10 (45.5) | RP1 (3), KLHL7 (2), PRPF31 (2), NRL (1), RHO (1), Unknown (1) | |||||
| XLRP | 2 (9.1) | RPGR (2) | |||||
| USH | 2 (9.1) | CLRN1 (1), USH2A (1) | |||||
| Mean |
Standard Deviation |
Quantile | |||||
| Minimum | 25th | Median | 75th | Maximum | |||
|
Follow-up time (yr) |
2.23 | 1.62 | 0.25 | 0.88 | 1.65 | 3.19 | 5.27 |
Data are summarized as mean ± standard deviation where appropriate. ARRP = autosomal recessive retinitis pigmentosa; ADRP = autosomal dominant retinitis pigmentosa; XLRP = X- linked retinitis pigmentosa; USH = Usher syndrome.