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172 Possible Causes for X-Linked Lymphoproliferative Disorder

  • Infectious Mononucleosis

    lymphoproliferative disorders are at highest risk of fulminant EBV infection. 29 A registry of 157 males with X-linked lymphoproliferative syndrome demonstrated a 96% mortality[aafp.org] Individuals with Duncan syndrome (ie, X-linked lymphoproliferative syndrome) may develop fatal primary Epstein-Barr virus infection due to a defect in the immune response[emedicine.com] […] syndrome showed a trend toward a higher risk of needing consultation for airway management in children younger than six years. 30 Patients who are immunocompromised or have X-linked[aafp.org]

  • X-Linked Lymphoproliferative Disorder

    X-linked lymphoproliferative disorder typically presents as an Epstein-Barr virus-specific immune defect with a poor prognosis.[ncbi.nlm.nih.gov] X-linked lymphoproliferative disorder is a rare immune disorder caused by genetic mutations on the X chromosome.[disability-benefits-help.org] SH2D1A gene defects are the cause of X-linked lymphoproliferative disorder (XLP-1), a rare condition characterized by severe immune dysregulation.[ncbi.nlm.nih.gov]

  • Lymphoproliferative Syndrome 1

    X-linked lymphoproliferative disease (also known as "Duncan's disease" [1] : 86 or "Purtilo syndrome" [2] ) is a lymphoproliferative disorder. [3] Presentation [ edit ] Strangely[en.wikipedia.org] Search Autoimmune lymphoproliferative syndrome Autoimmune lymphoproliferative syndrome (ALPS) is an inherited disorder in which the body cannot X-linked lymphoproliferative[ghr.nlm.nih.gov] […] an X-linked recessive disorder), and ataxia telangiectasia.[en.wikipedia.org]

  • Lymphoproliferative Disorder

    Because X-linked lymphoproliferative syndrome is inherited as an X-linked recessive genetic trait, the disorder is usually fully expressed in males only.[rarediseases.org] Lymphoproliferative Disorders. emedicine. Last Updated: April 7, 2006. 5pp. www.emedicine.com/ped/topic1345.htm[rarediseases.org] XLP2 is caused by mutations in a gene that encodes the X-linked inhibitor of apoptosis protein (XIAP).[merckmanuals.com]

  • Agammaglobulinemia

    X-linked agammaglobulinemia, common variable immunodeficiency, Chediak-Higashi syndrome, Wiskott-Aldrich syndrome, and X-linked lymphoproliferative disorder.[journals.lww.com] (CDG-IIb), X-linked lymphoproliferative disorder, and TRNT1 can all cause hypogammaglobulinemia.[invitae.com] ., common variable immunodeficiency, Chediak-Higashi syndrome, Wiskott-Aldrich syndrome and X-linked lymphoproliferative disorder, are 100-300 times the rate in the normal[journals.lww.com]

  • Acute Panmyelosis with Myelofibrosis

    disorder Thrombophilia due to myeloproliferative disorder Virus-associated atypical lymphoproliferative disorder X-linked lymphoproliferative syndrome Clinical Information[icd9data.com] disorder Thrombophilia due to myeloproliferative disorder Virus-associated atypical lymphoproliferative disorder X-linked lymphoproliferative syndrome Applies To Lymphoproliferative[icd9data.com] Fatal infectious mononucleosis associated with X-linked lymphoproliferative syndrome Fungating tumor of lymph node Hematologic neoplasm of uncertain behavior Hemolytic anemia[icd9data.com]

  • Primary Immune Deficiency Disorder

    Some of these include: Severe combined immunodeficiency Common variable immunodeficiency DiGeorge syndrome/22q11 microdeletion syndrome X-linked agammaglobulinemia/Bruton's[chw.org] Other, less severe CIDs that do not characteristically lead to early mortality include Wiskott-Aldrich syndrome, DiGeorge syndrome, ataxia-telangiectasia, and X-linked lymphoproliferative[aacijournal.biomedcentral.com] Autoimmune polyendocrinopathy candidiasis and ectodermal dystrophy, autoimmune lymphoproliferative syndrome, immunodyregulation polyendocrinopathy enteropathy X-linked, IL[link.springer.com]

  • X-Linked Hypogammaglobulinemia

    (CDG-IIb), X-linked lymphoproliferative disorder, and TRNT1 can all cause hypogammaglobulinemia.[invitae.com] […] glycosylation (CDG-IIb), X-linked lymphoproliferative disorder, and TRNT1 can all cause hypogammaglobulinemia.[invitae.com] Genes tested Primary panel BLNK BTK CD79A CD79B IGLL1 PIK3R1 Add-on Hypogammaglobulinemia Genes GATA2 MOGS SH2D1A TRNT1 XIAP GATA2 deficiency, MOGS-congenital disorder of[invitae.com]

  • Kostmann Syndrome

    Disorders (LPD) Lymphoproliferative Disorder, X-linked (also known as Epstein–Barr Virus Susceptibility) Wiskott–Aldrich Syndrome Myeloproliferative Disorders Acute Myelofibrosis[cryo-cell.com] B Cells Omenn Syndrome Kostmann Syndrome Ataxia–Telangiectasia Bare Lymphocyte Syndrome Common Variable Immunodeficiency DiGeorge Syndrome Leukocyte Adhesion Deficiency Lymphoproliferative[cryo-cell.com]

  • Adult Idiopathic Neutropenia

    […] agammaglobulinemia X-linked hyper-IgM syndrome X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia X-linked immunoneurologic disorder[se-atlas.de] X-linked lymphoproliferative disease X-linked mendelian susceptibility to mycobacterial diseases X-linked mendelian susceptibility to mycobacterial diseases due to CYBB deficiency[se-atlas.de] […] fever/inflammatory syndrome Unexplained periodic fever syndrome of childhood Unspecified juvenile idiopathic arthritis Vici syndrome WHIM syndrome Wiskott-Aldrich syndrome X-linked[se-atlas.de]

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