Volume 23, Number 10—October 2017
Research
Poliovirus Excretion in Children with Primary Immunodeficiency Disorders, India
Table 1
Baseline characteristics of confirmed PID cases in children recruited from Wadia Children’s Hospital, Mumbai, India, September 2014–April 2017*
Serial no. | PID types | No. cases | M/F ratio | Age range, mo |
---|---|---|---|---|
1 | Hemophagocytic lymphohistiocytosis | 11 | 10/1 | 4–96 |
2 | X-linked agammaglobulinemia | 7 | 7/0 | 27–216 |
3 | Chronic granulomatous disease | 4 | 3/1 | 7–60 |
4 | Severe combined immunodeficiency | 4 | 4/0 | 4–48 |
5 | Common variable immunodeficiency | 3 | 2/1 | 84–120 |
6 | Chédiak–Higashi syndrome | 3 | 1/2 | 26–86 |
7 | Hypogammaglobulinemia | 2 | 1/1 | 96–108 |
8 | IgG subclass deficiency | 2 | 0/2 | 84–114 |
9 | Hyper-IgM syndrome | 2 | 2/0 | 17–59 |
10 | Autoimmune lymphoproliferative syndrome | 1 | 0/1 | 15 |
11 | B cell expansion with NF-κB and T cell anergy | 1 | 1/0 | 18 |
12 | Hyper-IgE syndrome | 1 | 1/0 | 42 |
13 |
Interleukin 12 receptor β1 defect |
1 |
1/0 |
156 |
Total | 42 | 33/9 | 4–216 |
*PID, primary immunodeficiency