The patient with Wiskott-Aldrich syndrome has severe bleeding and inflammation both in the middle ear cavity and in the inner ear. Cochlear damage may be one of the causes of hearing loss in Wiskott-Aldrich syndrome. Decreased immune response increases the tendency for otitis media and its inner ear interactions.
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What are the three features of Wiskott-Aldrich syndrome?
What are the symptoms of Wiskott-Aldrich syndrome?
What are the manifestations of Wiskott-Aldrich syndrome?
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Wiskott-Aldrich syndrome is a rare genetic immunodeficiency that keeps a child's immune system from functioning properly.
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The deafness arising in patients suffering from the Wiskott-Aldrich-syndrome represents a so far not described symptom of that illness.
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Dec 1, 2019 · Wiskott-Aldrich syndrome is characterized by abnormal immune system function (immune deficiency), eczema (an inflammatory skin disorder)
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Wiskott-Aldrich syndrome (WAS) is a rare primary immunodeficiency (PI) that causes bleeding problems and eczema in addition to susceptibility to infections.
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Wiskott Aldrich syndrome (WAS) is a disease with immunological deficiency and reduced ability to form blood clots.
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Wiskott-Aldrich syndrome is an immunodeficiency disorder that causes frequent infections, abnormal bleeding, autoimmune problems and rashes like eczema.
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Sep 4, 2024 · Wiskott-Aldrich syndrome (WAS) is an X-linked disorder characterized by the clinical triad of microthrombocytopenia, eczema, and recurrent infections.
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Oct 1, 2024 · Wiskott-Aldrich syndrome is a rare genetic disorder affecting the male immune system. The classic signs include recurring infections, eczema, and decreased ...
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Summary. Wiskott]Aldrich syndrome (WAS) covers a group of rare serious disorders affecting about 4 people in a million and usually affects only males.
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