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Results 1 - 10 of 100 for hies
  1. Hyper-Immunoglobulin E Syndromes (HIES) From the National Institutes of Health (National Institute of Allergy and Infectious Diseases)  
    NIAID studies many different syndromes which lead to high levels of an antibody called immunoglobulin E and are collectively called hyper-IgE syndromes.
    https://www.niaid.nih.gov/.../hyper-immunoglobulin-e-syndromes-hies - External Health Links
  2. DOCK8 immunodeficiency syndrome 
    ... show signs and symptoms of the condition. AR-HIES Autosomal recessive HIES Autosomal recessive hyper-IgE syndrome CID due to ...
    https://medlineplus.gov/.../dock8-immunodeficiency-syndrome - Genetics
  3. Autosomal dominant hyper-IgE syndrome 
    Autosomal dominant hyper-IgE syndrome (AD-HIES), formerly known as Job syndrome, is a condition that affects several body systems, particularly the immune system. Recurrent infections are common in ...
    https://medlineplus.gov/.../autosomal-dominant-hyper-ige-syndrome - Genetics
  4. Types of Primary Immune Deficiency Diseases From the National Institutes of Health (National Institute of Allergy and Infectious Diseases)  
    Immune System and Disorders/Specifics ... Immune System and Disorders ... National Institute of Allergy and Infectious Diseases ... From the National Institutes of Health
    https://www.niaid.nih.gov/diseases-conditions/types-pidds - External Health Links
  5. PGM3-congenital disorder of glycosylation 
    PGM3-congenital disorder of glycosylation (PGM3-CDG) is an inherited condition that primarily affects the immune system but can also involve other areas of ...
    https://medlineplus.gov/...pgm3-congenital-disorder-of-glycosylation - Genetics
  6. Congenital sucrase-isomaltase deficiency 
    ... DM, Wanes D, Marten LM, Zimmer KP, Naim HY. Heterozygotes Are a Potential New Entity among Homozygotes ... PubMed Jacob R, Zimmer KP, Schmitz J, Naim HY. Congenital sucrase-isomaltase deficiency arising from cleavage and ...
    https://medlineplus.gov/.../congenital-sucrase-isomaltase-deficiency - Genetics
  7. MECP2 gene 
    ... IB, Wan M, Tran CQ, Francke U, Zoghbi HY. Rett syndrome is caused by mutations in X- ... 00624-0. Citation on PubMed Chahrour M, Zoghbi HY. The story of Rett syndrome: from clinic to ...
    https://medlineplus.gov/genetics/gene/mecp2 - Genetics
  8. SI gene 
    ... DM, Wanes D, Marten LM, Zimmer KP, Naim HY. Heterozygotes Are a Potential New Entity among Homozygotes ... PubMed Jacob R, Zimmer KP, Schmitz J, Naim HY. Congenital sucrase-isomaltase deficiency arising from cleavage and ...
    https://medlineplus.gov/genetics/gene/si - Genetics
  9. STAT3 gene 
    ... people with autosomal dominant hyper-IgE syndrome (AD-HIES), a disorder of the immune system that leads ... Changes in the STAT3 gene that cause AD-HIES alter the structure and function of the STAT3 ...
    https://medlineplus.gov/genetics/gene/stat3 - Genetics
  10. Familial paroxysmal nonkinesigenic dyskinesia 
    ... NONKINESIGENIC DYSKINESIA 2; PNKD2 PubMed Bruno MK, Lee HY, Auburger GW, Friedman A, Nielsen JE, Lang AE, ... PubMed or Free article on PubMed Central Lee HY, Xu Y, Huang Y, Ahn AH, Auburger GW, ...
    https://medlineplus.gov/...lial-paroxysmal-nonkinesigenic-dyskinesia - Genetics
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