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Results 1 - 10 of 15 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. 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
  5. 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
  6. 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
  7. X-linked agammaglobulinemia 
    ... are usually healthy for the first 1 or 2 months of life because they are protected by ... the X chromosome, which is one of the two sex chromosomes. In males (who have only one ...
    https://medlineplus.gov/.../condition/x-linked-agammaglobulinemia - Genetics
  8. Trichothiodystrophy 
    ... group of proteins called the general transcription factor 2 H (TFIIH) complex. This complex is involved in ... Registry: Trichothiodystrophy 1, photosensitive Genetic Testing Registry: Trichothiodystrophy 2, photosensitive Genetic Testing Registry: Trichothiodystrophy 3, photosensitive Genetic ...
    https://medlineplus.gov/genetics/condition/trichothiodystrophy - Genetics
  9. X-linked hyper IgM syndrome 
    ... hyper IgM syndrome is estimated to occur in 2 per million newborn boys. Variants (also known as ... the X chromosome, which is one of the two sex chromosomes. In males (who have only one ...
    https://medlineplus.gov/.../condition/x-linked-hyper-igm-syndrome - Genetics
  10. ALG1-congenital disorder of glycosylation 
    ... 10.1136/jmg.2009.072504. Epub 2010 Aug 2. Erratum In: J Med Genet. 2015 Mar;52( ... early fatal outcome. Gene. 2014 Jan 25;534(2):345-51. doi: 10.1016/j.gene.2013. ...
    https://medlineplus.gov/...alg1-congenital-disorder-of-glycosylation - Genetics
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