Table 1.

Patients characteristics

CharacteristicsN = 28
Male 17 (60.7%) 
Age at PID diagnosis (y) 30 (14-68) 
Age at ITP diagnosis (y) 31 (5-68) 
Follow-up duration after ITP diagnosis (mo) 81 (11-324) 
Type of PID   
CVID 24 (85.7%) 
Including LOCID (10.7%) 
HIGM (3.6%) 
CTLA4 deficiency (3.6%) 
PI3KCD mutation (3.6%) 
KMT2D mutation (Kabuki syndrome) (3.6%) 
Immunoglobulin serum levels at the time of PID diagnosis (mg/dL)   
IgG 326 (85-486) 
IgA 27 (0-146) 
IgM 39 (4-500) 
CharacteristicsN = 28
Male 17 (60.7%) 
Age at PID diagnosis (y) 30 (14-68) 
Age at ITP diagnosis (y) 31 (5-68) 
Follow-up duration after ITP diagnosis (mo) 81 (11-324) 
Type of PID   
CVID 24 (85.7%) 
Including LOCID (10.7%) 
HIGM (3.6%) 
CTLA4 deficiency (3.6%) 
PI3KCD mutation (3.6%) 
KMT2D mutation (Kabuki syndrome) (3.6%) 
Immunoglobulin serum levels at the time of PID diagnosis (mg/dL)   
IgG 326 (85-486) 
IgA 27 (0-146) 
IgM 39 (4-500) 

Normal values (ranges): IgG, 650 to 1400 mg/dL; IgA, 70 to 320 mg/dL; IgM, 50 to 350 mg/dL. Quantitative variables are presented as median (range, minimum to maximum) and qualitative variables as frequency (percentage).

HIGM, hyper IgM syndrome; LOCID, late-onset combined immune deficiency.

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