Table 1.

Main characteristics of PID patients and schools

PID patients (N = 13) 
Age Median/IQR 13.8/13–15 
Sex M/F 8/5 
Level of functioning Level 0/1/2/3 4/3/4/2 
Treatment IgRT/SCT 6/1 
PID Dx X-linked agammaglobulinemia 
Ataxia telangiectasia 
Chronic granulomatous disease 
STAT3-LOF hyper IgE syndrome 
Autoimmune lymphoproliferative syndrome 
SAVI 
Combined immunodeficiencies with associated or syndromic features 
Autoinflammatory disorders (non-inflammasome-related conditions) 
Predominantly antibody deficiencies (severe reduction in at least two serum immunoglobulin isotypes with a normal or low number of B cells, CVID phenotype) 
Frequency of psychology visits Weekly/monthly/quarterly 2/7/4 
Parents (N = 21) Father/mother 9/12 
Schools (N = 13) 
Type of school Public/private 11/2 
Prior school coordination Yes/no 9/4 
Schools with classmate participation Yes/no 9/4 
Classmates (N = 74) Male/female/non-binary 34/39/1 
PID patients (N = 13) 
Age Median/IQR 13.8/13–15 
Sex M/F 8/5 
Level of functioning Level 0/1/2/3 4/3/4/2 
Treatment IgRT/SCT 6/1 
PID Dx X-linked agammaglobulinemia 
Ataxia telangiectasia 
Chronic granulomatous disease 
STAT3-LOF hyper IgE syndrome 
Autoimmune lymphoproliferative syndrome 
SAVI 
Combined immunodeficiencies with associated or syndromic features 
Autoinflammatory disorders (non-inflammasome-related conditions) 
Predominantly antibody deficiencies (severe reduction in at least two serum immunoglobulin isotypes with a normal or low number of B cells, CVID phenotype) 
Frequency of psychology visits Weekly/monthly/quarterly 2/7/4 
Parents (N = 21) Father/mother 9/12 
Schools (N = 13) 
Type of school Public/private 11/2 
Prior school coordination Yes/no 9/4 
Schools with classmate participation Yes/no 9/4 
Classmates (N = 74) Male/female/non-binary 34/39/1 

To calculate the patient’s level of functioning, we used the Eastern Cooperative Oncology Group performance status scale (19). CVID, Common variable immunodeficiency; Dx, diagnosis; IgRT, immunoglobulin replacement therapy; SAVI, STING-associated vasculopathy with onset in infancy; SCT, stem cell transplantation.

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