the Syndrome Wiskott-Aldrich syndrome is a rare disease that affects boys. The discovery of the disease in women are rare, and associated with impaired activity of the X chromosome. Disease meets at approximately 4% of children in 1 million live births. Women can act as carriers of the disease.
the Syndrome has a high mortality rate, most patients do not survive to 5 years. The patient has bleeding disorders, eczema, bloody diarrhea. Patients exposed to any viral or bacterial diseases.
the Syndrome Wiskott-Aldrich syndrome is a genetic X-linked disease characterized by eczema, thrombocytopenia. Diagnosed after conducting DNA-analysis.
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