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Possible Causes For Hypogammaglobulinemia, acquired - Causes
- Infectious Disorders (Specific Agent)
Immune deficiency , acquired (AIDS/HIV)- Neoplastic Disorders
Chronic Lymphocytic Leukemia CLL
Leukemia
Leukemia, chronic
Myelogenous leukemia, chronic
Thymoma
Thymoma with immunodeficiency- Allergic, Collagen, Auto-Immune Disorders
Lupus nephritis
Nephrotic syndrome
Lupus erythematosis, systemic- Metabolic, Storage Disorders
Amyloidosis, renal- Deficiency Disorders
Kwashiorkor (protein deficiency,severe)- Congenital, Developmental Disorders
Mucocutaneous candidiasis, chronic syn
IgG deficiency, selective
Immundeficiency, combined B And T cell
Primary protein losing enteropathy syndrome- Hereditary, Familial, Genetic Disorders
Hypogammaglobulinemia, cong. X-linked
Ataxia-telangiectasia
X-linked Lymphoproliferative Syndrome (Duncan)
Severe combined immunodeficiency synd/SCID
Nezelof syndrome (Combined Immune deficiency var)- Anatomic, Foreign Body, Structural Disorders
Pleural chylous effusion- Reference to Organ System
Agammaglobulinemia, acquired
Protein losing enteropathy
Dysgammaglobulinemia, type 1
Hypogammaglobulinemia/Agammaglobulinemia
Immunodeficiency (common variable)- Pathophysiologic
B-cell injury or lesion- Drugs
Immunosuppressive drugs/Administration/Toxicity
Corticosteroid Administration/Toxicity
Chlorpromazine (Thorazine) Administration/Toxicity
Phenytoin (Dilantin) Administration/Toxicity- Synonyms
- Secondary acquired hypogammaglobulinaemia, Secondary acquired hypogammaglobulinemia
- Definition
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- External Links Related to Hypogammaglobulinemia, acquired - Causes
- Wikipedia
- Merck
- Images
- PubMed (National Library of Medicine)
- NGC (National Guideline Clearinghouse)
- Medscape (eMedicine)
- Harrison's Online (accessmedicine)
- NEJM (The New England Journal of Medicine)