Wiskott-Aldrich syndrome: Difference between revisions
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Created page with "* Primary immunodeficiency * X-linked recessive defect in the WAS gene located at xP 11.22-23 * Characterized by eczema, thrombocytopenia, immunodeficiency Category:Genetic syndromes Category:Immunodeficiencies" |
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* [[Primary immunodeficiency]] |
* [[Primary immunodeficiency]] |
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* X-linked recessive defect in the |
* X-linked recessive defect in the WASp gene located at xP 11.22-23 |
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* Characterized by [[eczema]], [[thrombocytopenia]], [[immunodeficiency]] |
* Characterized by [[eczema]], [[thrombocytopenia]] (causing bleeding), and [[immunodeficiency]] |
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** Immunodeficiency is characterized by recurrent infections with encapsulated organisms and recurrent sinopulmonary infections |
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** Myeloid cells have impaired phagocytosis and chemotaxis; also have issues with T cell and B cell dysfunction |
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[[Category:Genetic syndromes]] |
[[Category:Genetic syndromes]] |
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Latest revision as of 20:20, 6 October 2025
- Primary immunodeficiency
- X-linked recessive defect in the WASp gene located at xP 11.22-23
- Characterized by eczema, thrombocytopenia (causing bleeding), and immunodeficiency
- Immunodeficiency is characterized by recurrent infections with encapsulated organisms and recurrent sinopulmonary infections
- Myeloid cells have impaired phagocytosis and chemotaxis; also have issues with T cell and B cell dysfunction
