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. Author manuscript; available in PMC: 2013 Jun 24.
Published in final edited form as: J Clin Immunol. 2012 Sep 1;33(1):40–48. doi: 10.1007/s10875-012-9773-1

Table IV.

Admissions of patients with PID as a primary or secondary diagnosis

PID code and description Admissions Percent
Hypogammaglobulinemia unspecified 924 22.13 %
Unspecified immunity deficiency 531 12.72 %
Common variable Immunodeficiency 495 11.85 %
DiGeorge’s syndrome 448 10.73 %
Selective deficiency IgG 441 10.56 %
Selective IgA Immunodeficiency 274 6.56 %
Combined immunodeficiency (includes SCID) 247 5.91 %
Single Complement 239 5.72 %
Immunodeficiency with predominant T-cell
defect
197 4.72 %
Unspecified disorder of immune mechanism 151 3.62 %
Wiskott-Aldrich syndrome 121 2.90 %
Congenital hypogammaglobulinemia
(Agammaglobulinemia)
36 0.86 %
Selective IgM Immunodeficiency 32 0.77 %
Transient hypogammaglobulinemia 20 0.48 %
Hyper-IgM 18 0.43 %
Nezelof’s syndrome 2 0.05 %
4,176 100.0 %