Table 4

Type of PHID and PHID complications in 5 clusters of 79 PHID patients, ALTADIH Cohort, 2007-2010
Cluster 1 Cluster 2 Cluster 3 Cluster 4 Cluster 5
n = 33 n = 18 n = 4 n = 8 n = 16
n % n % n % n % n %
Type of PHID
     CVID 23 (70) 8 (44) 3 (75) 8 (100) 13 (82)
     IgG subclass deficiency 10 (30) 10 (56) 0 (0) 0 (0) 1 (6)
     Good’s syndrome 0 (0) 0 (0) 1 (25) 0 (0) 2 (12)
PHID complications (at least one of the following) 5 (15) 6 (33) 3 (75) 7 (88) 10 (63)
     Lymphoid hyperplasia 2 (6) 5 (28) 1 (25) 3 (38) 5 (31)
     Splenomegaly 1 (3) 2 (11) 1 (25) 7 (88) 3 (19)
     Autoimmune manifestations 3 (9) 1 (5) 1 (25) 2 (25) 7 (44)
     Granulomatous disease 0 (0) 1 (5) 2 (50) 4 (50) 2 (13)
     Villous atrophy 0 (0) 2 (11) 0 (0) 0 (0) 3 (19)
     Chronic inflammatory intestinal disease 0 (0) 2 (11) 1 (25) 1 (13) 0 (0)

Picat et al.

Picat et al. BMC Immunology 2014 15:13   doi:10.1186/1471-2172-15-13

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