Table 1.
n = 120 for cohort | |
---|---|
Age at end of study period (yr) | 52 ± 19 (2–87) |
Sex | |
Male | 32 (27%) |
Female | 88 (73%) |
Race | |
White | 97 (81%) |
Black | 6 (5%) |
Hispanic | 6 (5%) |
Asian | 3 (3%) |
Other/not recordeda | 8 (7%) |
Age at onset of hypoparathyroidism (yr) | 35 ± 21 (0–76) |
Duration of hypoparathyroidism (yr) | 17 ± 16 (1–59) |
Etiology | |
Total acquired | 107 (89%) |
Postsurgical | 79 (66%) |
Autoimmune | 9 (7%) |
Idiopathic (acquired) | 19 (16%) |
Total congenital | 13 (11%) |
Activating CaSR mutation | 5 (4%) |
DiGeorge syndrome | 3 (3%) |
Kearns-Sayre syndrome | 1 (1%) |
Idiopathic (congenital) | 4 (3%) |
Data are presented as mean ± sd (range) for age at end of study period, age at onset, and duration of hypoparathyroidism. Data are presented as n (percent) for subgroup totals.
Includes American Indian (n = 1), other (n = 1), and not recorded (n = 6).