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. 2022 Aug 31;11(17):5163. doi: 10.3390/jcm11175163

Table 1.

Patients’ characteristics and otitis media history.

PCD 1 Group
N = 17
Control Group
N = 17
p-Value
Age, median (Q1–Q3) 39 (33–54) 39 (33–54) 0.89
Gender male, n (%) 8 (47%) 6 (35%) 0.49
Ciliary ultrastructure defect, n (%)
nEM 2 5 (29%) 17 (100%) -
IDA + MTD 3 3 (18%) 0 -
ODA 4 6 (35%) 0 -
IDA + ODA 3 (18%) 0 -
CC 5 0 0 -
Kartagener syndrome, n (%) 3 (18%) 0 0.22
Consanguinities, n (%) 8 (47%) 3 (18%) 0.07
Otitis media history, n (%) 10 (59%) 3 (18%) 0.01
Rhinosinusitis history, n (%) 17 (100%) 13 (76%) 0.1
CRSwNP 6, n(%) 7 (41%) 2 (12%) 0.1
SNOT-22 7 score, median (Q1–Q3) 58 (46.5–69) 33.5 (14.2–46) 0.01
Sinus hypo or aplasia, n (%) 15 (88%) 3 (18%) 0.0001
Modified Lund–Mackay score, median (Q1–Q3) 13.5 (10–19.2) 6 (2.7–10.2) 0.01

1 Primary ciliary dyskinesia; 2 normal electronic microscopy; 3 inner dynein arm defects with microtubular disorganization; 4 outer dynein arm defects; 5 central complex defects, 6 chronic rhinosinusitis with nasal polyps, 7 sinonasal outcome test-22.