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Results 1 - 10 of 21 for Immunoglobulin A deficiency 2
  1. Common variable immune deficiency 
    ... R. New diagnostic criteria for common variable immune deficiency (CVID), which may assist with decisions to treat with intravenous or subcutaneous immunoglobulin. Clin Exp Immunol. 2013 Nov;174(2):203-11. doi: 10.1111/cei.12178. Citation ...
    https://medlineplus.gov/.../common-variable-immune-deficiency - Genetics
  2. DOCK8 immunodeficiency syndrome 
    ... Hyper IgE recurrent infection syndrome, autosomal recessive Hyper immunoglobulin E syndrome, autosomal recessive ... due to DOCK8 deficiency National Organization ...
    https://medlineplus.gov/.../dock8-immunodeficiency-syndrome - Genetics
  3. Purine nucleoside phosphorylase deficiency 
    ... Purine nucleoside phosphorylase deficiency with fatal course in two sisters. Eur J ... Resembling IgA Deficiency and a Review of the Literature. Immunol Invest. ...
    https://medlineplus.gov/...urine-nucleoside-phosphorylase-deficiency - Genetics
  4. PNP gene 
    ... Purine nucleoside phosphorylase deficiency with fatal course in two sisters. Eur J ... Resembling IgA Deficiency and a Review of the Literature. Immunol Invest. ...
    https://medlineplus.gov/genetics/gene/pnp - Genetics
  5. IFIH1 gene 
    ... Am J Hum Genet. 2015 Feb 5;96(2):275-82. doi: 10.1016/j.ajhg.2014.12.014. Epub ... With Selective IgA Deficiency. Arthritis Rheumatol. 2015 Jun;67(6):1592-7. ...
    https://medlineplus.gov/genetics/gene/ifih1 - Genetics
  6. PLCG2 gene 
    ... for making an enzyme called phospholipase C gamma 2 (PLCγ2). This enzyme performs a chemical reaction that ... PLAID. More About This Health Condition At least two mutations in the PLCG2 gene cause a condition ...
    https://medlineplus.gov/genetics/gene/plcg2 - Genetics
  7. TNFRSF13B gene 
    ... coding variants in common variable immunodeficiency and selective IgA deficiency. Nat Genet. 2007 Apr;39(4):429-30. ...
    https://medlineplus.gov/genetics/gene/tnfrsf13b - Genetics
  8. X-linked lymphoproliferative disease 
    ... from hemophagocytic lymphohistiocytosis.XLP can be divided into two types based on its genetic cause and pattern ... the X chromosome, which is one of the two sex chromosomes. In males (who have only one ...
    https://medlineplus.gov/.../x-linked-lymphoproliferative-disease - Genetics
  9. Anhidrotic ectodermal dysplasia with immune deficiency 
    ... inflammatory bowel disease or rheumatoid arthritis.There are two forms of EDA-ID that have similar signs ... dominant EDA-ID. The proteins produced from these two genes regulate nuclear factor-kappa-B. Nuclear factor- ...
    https://medlineplus.gov/...todermal-dysplasia-with-immune-deficiency - Genetics
  10. TRNT1 deficiency 
    ... individuals, the episodes occur regularly, arising approximately every 2 to 4 weeks and lasting 5 to 7 ... deficiency encompasses what was first thought to be two separate disorders, a severe disorder called sideroblastic anemia ...
    https://medlineplus.gov/genetics/condition/trnt1-deficiency - Genetics
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