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Immunodeficiency syndromes
Wiskott aldrich

Wiskott aldrich

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Wiskott-Aldrich syndrome is a rare, inherited condition due to a disorder of the blood cells and cells of the immune system. It occurs primarily in males. Common signs in infants are easily bruising, spontaneous nosebleeds, bloody diarrhea, and eczema.

Dr. Geoffrey Rutledge reviewed this

39 year experience in Internal Medicine

Is a type of:

Genetic disease • Hemorrhagic disorders • Immunodeficiency syndromes

How long it usually lasts:

Chronic (lasts years to lifelong)

How common it is:

Very rare

Symptoms

Bruising
Swollen glands
Bruising easily
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Medications

Ratings show how effective doctors think these medications are at treating Wiskott aldrich
Immunosuppressive therapy
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Procedures

Ratings show how effective doctors think these procedures are at treating Wiskott aldrich

Surgery

Bone marrow transplant
3.7
11 reviews
Splenectomy
2.8
10 reviews

Other treatments

Watchful waiting
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Tests

Liver function test
Complete blood count
Total lymphocyte enumeration
T cell proliferation assay
Wiskott aldrich syndrome protein mutation analysis
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Related questions

A 37-year old asked:

What are the tests for wiskott aldrich?

2 doctor answers • 2 doctors weighed in

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Do wiskott aldrich kids grow into adulthood, and if so, what symptoms do wiskott aldrich adults have? How do the adults differ from the kids?

2 doctor answers • 2 doctors weighed in

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Why does wiskott aldrich syndrome only affect males?

2 doctor answers • 4 doctors weighed in

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2 doctor answers • 3 doctors weighed in

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2 doctor answers • 3 doctors weighed in

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1 doctor answer • 1 doctor weighed in

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