Table 1.
Total | Male | Female | P | |
---|---|---|---|---|
Screened SDHB mutation carriers (N, %) | 241 (100%) | 111 (46.06%) | 130 (53.94%) | 0.25 |
Age of initial screening* | 38 (2 – 85) | 40 (2 – 85) | 37.5 (3 – 83) | 0.80 |
Years of screening/follow-up at NIH* | 1 (0-14) | 2 (0 – 11) | 1 (0 – 14) | 0.11 |
Number of screenings/follow-ups* | 2 (1-26) | 2 (1 – 26) | 2 (1 – 10) | 0.11 |
Other tumors (N, %) | 27 (11.20%) | 15 (13.51%) | 12 (9.23%) | 0.20 |
PHEO/PGL diagnosis | 40 (16.60%) | 27 (24.32%) | 13 (10.00%) | 0.003 |
Age at initial diagnosis* | 36.5 (11 – 74) | 34 (11 – 74) | 44 (13 – 64) | 0.56 |
Diagnosed at initial screening (N, %) | 23 (57.50%) | 18 (66.67%) | 5 (38.46%) | 0.17 |
Diagnosed prior coming to NIH | 14 (35%) | 8 (29.63%) | 6 (46.15%) | 0.48 |
years, median (range)