Drug Induced
|
|
Antimalarial agents |
|
Captopril |
|
Carbamazepine |
|
Glucocorticoids |
|
Fenclofenac |
|
Gold salts |
|
Penicillamine |
|
Phenytoin |
|
Sulphasalazine |
|
|
Genetic Disorders
|
|
Ataxia - Telangiectasia |
|
Autosomal forms of SCID |
|
Hyper IgM Immunodeficiency |
|
transcobalamin II deficiency and hypogammaglobulineinia |
|
X-linked agammaglobulinemia |
|
X-linked lyinphoproliferative disorder (EBY associated) |
|
X-linked SCID |
|
Some metabolic disorders |
|
|
Chromosomal Anomalies
|
|
Chromosome 18q- Syndrome |
|
Monosomy 22 |
|
Trisomy 8 |
|
Trisomy 21 |
|
|
Infectious Diseases
|
|
HIV |
|
Congenital Rubella |
|
Congenital infection with CMV |
|
Congenital infection with Toxoplasma gondii |
|
Epstein-Barr Virus |
|
|
Malignancy
|
|
Chronic Lymphocytic Leukemia |
|
Immunodeficiency with Thymoma |
|
Non Hodgkin's lymphoma |
|
B cell malignancy |
|
|
Systemic Disorders
|
|
Immunodeficiency caused by hypercatabolism of immunoglobulin |
|
Immunodeficiency caused by excessive loss of immunoglobulins (nephrosis,
severe burns, lymphangiectasia, severe diarrhea) |