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1,208 Possible Causes for WAS

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  • Malignant Neoplasm

    Ann Thorac Surg. 2017 May;103(5):e405-e407. doi: 10.1016/j.athoracsur.2016.10.045. Author information 1 Department of Pathology, Dartmouth Hitchcock Medical Center, Lebanon, New Hampshire. 2 Department of Surgery, Dartmouth Hitchcock Medical Center, Lebanon, New Hampshire. 3 Department of Radiology, Dartmouth[…][]

  • Thrombocytopenia

    Abstract Renal involvement is occasionally observed in Wiskott-Aldrich syndrome (WAS) and X-linked thrombocytopenia (XLT).[] […] there is a reduced number of thrombocytes ( blood . 2 Causes There exists a wide range of causes for thrombocytopenias: Formation disorders Congenital formation disorders Wiskott-Aldrich[] Wiskott-Aldrich Syndrome (see this term) should also be excluded. Antenatal diagnosis Prenatal diagnosis is possible in families with a known GATA1 mutation.[]

  • Immunodeficiency Syndrome, Variable

    Vancouver @article{df09914890354d2985ca9bbc6ae9d04f, title "Immunodeficiency syndromes: X-linked agammaglobulinemia, common variable immunodeficiency, Chediak-Higashi syndrome, Wiskott-Aldrich[] Detection of WAS (Wiskott-Aldrich Syndrome) protein. PID screening and specialised diagnostic tests are appointment based tests.[] SR-Tiget is also most satisfied at the results of its work on children presenting metachromatic leukodystrophy, a neurodegenerative disease, and Wiskott-Aldrich syndrome,[]

  • Acute Lymphoblastic Leukemia

    Although a few cases are associated with inherited genetic syndromes (eg, Down syndrome ) or congenital immunodeficiencies (eg, Wiskott-Aldrich syndrome , ataxia-telangiectasia[] Down syndrome, Wiskott-Aldrich syndrome, ataxia-telangiectasia and neurofibromatosis.[] Children with various primary immunodeficiencies, including severe combined immunodeficiency, X-linked agammaglobulinemia, and Wiskott-Aldrich syndrome, as well as those receiving[]

  • Velocardiofacial Syndrome

    […] pigmentosum 707 262 Cutis marmorata teleangiectatica congenita 709 263 Cutis marmorata teleangiectatica congenita und Makrozephalie 711 264 Morbus Abt-Letterer-Siwe 713 265 Wiskott-Aldrich-Syndrom[] Glomerulosklerose Kimmelstiel-Wilson-Syndrom Winter-Kohn-Mellmann-Wagner-Syndrom / Winter-Syndrom Schleudertrauma Whiplash-Syndrom Thalidomid- Embryopathie Widemann-Dysmaliesyndrom Wiskott-Aldrich-Syndrom[]

  • Campylobacter Enteritis

    We also report two typically mild cases of C. enteritis, a newborn infant with monosymptomatic bleeding in stools and diarrhea, and another 11-month-old, Wiskott-Aldrich syndrome[]

  • Thoracic Aortic Aneurysm

    Abstract An association has been reported between Wiskott-Aldrich syndrome and necrotizing vasculitis and aneurysmal arterial dilatation.[] We present here the first endovascular repair of descending thoracic aortic aneurysm in a 35-year-old male patient with the classical Wiskott-Aldrich syndrome phenotype.[]

  • Acquired Angioedema

    X-linked agammaglobulinemia Transient hypogammaglobulinemia of infancy Dysgammaglobulinemia IgA deficiency IgG deficiency IgM deficiency Hyper IgM syndrome ( 1 2 3 4 5 ) WiskottAldrich[] syndrome Hyper-IgE syndrome Other Common variable immunodeficiency ICF syndrome T cell deficiency ( T ) thymic hypoplasia : hypoparathyroid ( Di George's syndrome ) euparathyroid[]

  • Lambert Eaton Myasthenic Syndrome

    The common duplicated region in those three patients and the presented case comprises 12 disease-associated genes including the FOXP3 (Forkhead Box P3) and WAS (Wiskott-Aldrich[] syndrome) gene, both implicated in immune function.[]

  • Wiskott Aldrich Syndrome

    Thus, his disease was reclassified as Wiskott-Aldrich syndrome, class 5.[] Syndrome/genetics Wiskott-Aldrich Syndrome/immunology* Wiskott-Aldrich Syndrome/metabolism Wiskott-Aldrich Syndrome Protein/genetics Substances Antigens, CD19 CD19 molecule[] Syndrome/immunology Wiskott-Aldrich Syndrome/therapy* Wiskott-Aldrich Syndrome Protein/deficiency Wiskott-Aldrich Syndrome Protein/genetics Wiskott-Aldrich Syndrome Protein[]

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