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 % |