Unspecified hypogammaglobulinemia
Unspecified hypogammaglobulinemia refers to individuals who have low serum immunoglobulins but do not fit the diagnostic criteria of defined antibody deficiencies like common variable immune deficiency (CVID).
Veno-occlusive disease with immunodeficiency
Patients with veno-occlusive disease with immunodeficiency (VODI) have a predisposition to fungal infections, low platelet counts, and enlarged livers.
X-linked lymphoproliferative (XLP) syndromes 1 and 2
XLP is characterized by life-long vulnerability to Epstein-Barr virus (EBV) infection, which can lead to severe and fatal infectious mononucleosis, lymph node cancers (lymphomas), and combined immunodeficiency.
Chronic mucocutaneous candidiasis (CMC)
Chronic mucocutaneous candidiasis (CMC) is characterized by persistent Candida (fungus) infections of the mucous membranes, scalp, skin, and nails.
Immunoglobulin product booklet
Use this guide to compare immunoglobulin products approved for use in the U.S.
Sumitomo Pharma Co., Ltd.
Rethymic
Allogeneic processed thymus tissue–agdc.
Approved to treat: Congenital athymia.
Report side effects/adverse reactions at 833-369-9868.
ZAP-70 deficiency
ZAP-70 deficiency is a rare autosomal recessive combined immunodeficiency. Peripheral T cells from individuals with ZAP-70 deficiency demonstrate defective T cell signaling and have an autoreactive phenotype. Indeed, several individuals have presented with autoimmune disorders.
X-linked immunodeficiency with magnesium defect, EBV infection, and neoplasia (XMEN)
X-linked immunodeficiency with magnesium defect, EBV infection, and neoplasia (XMEN) is seen in boys and is characterized by low CD4 T cells, chronic Epstein-Barr virus (EBV) infections, and lymphoproliferative disorders related to the EBV.
