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. 2007 Aug 1;30(8):969–973. doi: 10.1093/sleep/30.8.969

Table 1.

Demographic and Clinical Data

N+ Cataplexy N+ Cataplexy N− Cataplexy Idiopathlc CNS Controls
Low hcrt Normal hcrt Hypersomnia
n = 31 n = 16 n = 7 n = 10 n = 50
Female/male 20/11 12/4 3/4 8/2 27/23
Median age 59 (16–76) 46 (23–72) 35 (13–57) 39 (29–60) 40 (16–80)
Age at symptom onset 15 (4–50) 16 (5–50) 23 (4–55) 20 (4–20)
Duration of disorder 26 (1–60) 22.5 (9–50) 10 (2–30) 15 (5–25)
Hypnagogic hallucinations 20 (71%)* 15 (94%) 5 (71%) 7 (70%)
Sleep paralysis 19 (68%)* 15 (94%) 3 (42%) 3 (30%)
Patients with relatives with sleep disorder 11 (36%)*
(18 relatives)
7 (43%)
(14 relatives)
1 (14%)
(1 relative)
2 (20%)
(3 relatives)

Table 1 shows the number and median age of patients in each group, and median age at symptom debut and median duration of the disorder in each patient group. It also shows the number and percentage of patients in each group who reported hypnagogic hallucinations, sleep paralysis and relatives with similar sleep disorder. (*Number of patients reduced to 28 due to incomplete answers to the questionnaire). The total number of reported relatives in each group is given in brackets. N = Narcolepsy, hcrt = hypocretin-1