Wiskott Aldrich syndrome

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Contents

Used for

Aldrich syndrome, Wiskott syndrome

Broader Terms

congenital skin disorder, genetic disorder, inborn immunodeficiency, syndrome, thrombocytopenia

Related Terms

sex linked trait

Scope Note

rare x-linked immunodeficiency syndrome of young boys characterized by eczema, thrombocytopenic purpura and recurrent pyogenic infection; IGM levels are low and IGA and IGE levels are elevated; lymphoreticular malignancies are common.

Facts (generated by robot; please edit if you find it inaccurate)

  • Influencing FactorsPattern of inheritance The gene for Wiskott-Aldrich syndrome is found on the X chromosome.
  • Wiskott Aldrich Syndrome Important It is possible that the main title of the report Wiskott Aldrich Syndrome is not the name you expected.
  • The estimated incidence is 1:300,000 births, which means that one boy with Wiskott-Aldrich Syndrome is born about every three years in Sweden.
  • The thrombocytopenia of Wiskott Aldrich syndrome is not related to a defect in proplatelet formation.

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