Table 1.

Patient distribution with the underlying primary immune deficiency disorder n = 16

Primary immune deficiency disorder	Number of patients, n (%)
Severe combined immune deficiency (SCID) (T- B- NK+)	1 (6%)
ORAI 1 mutation immune deficiency	1 (6%)
Hyper IgM disorder (CD40LG mutation)	1 (6%)
Chediak-Higashi syndrome with HLH	1 (6%)
Mendelian susceptibility to mycobacterial disorders (MSMD)	2 (12%)
Griscelli syndrome with HLH	2 (12%)
Congenital hemophagocytic lymphohistiocytosis (HLH)	3 (18%)
Wiskott-Aldrich syndrome (WAS)	5 (31%)