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Wiskott-Aldrich Syndrome

Diseases of the Blood and Immune Mechanism

Wiskott-Aldrich syndrome is a rare X-linked recessive disease characterized by eczema, thrombocytopenia, immune deficiency, and bloody diarrhea. It is also sometimes called the eczema-thrombocytopenia-immunodeficiency syndrome, in keeping with Aldrich's original description of the condition in 1954.

Facts
Classification
Body System
Lymphatic or Immune System 1
ICD-10 Chapter
III: Diseases of the Blood and Blood-Forming Organs and Certain Disorders Involving the Immune Mechanism 1
Communicable or Non-communicable
Non-Communicable 2
Transmission Route
Non-Transmissible 3
Causative Agent
Causative Agent (category)
Genetic / Hereditary 4
First Described
1954 4
Sources
1. Wikipedia: ICD-10
WikipediaList of chapters, Chapter III
Quote, List of chapters, Chapter III
Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
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2. Wikipedia: Non-communicable disease
WikipediaNamed examples section
Quote, Named examples section
NCDs include Parkinson's disease, autoimmune diseases, strokes, heart diseases, cancers, diabetes, chronic kidney disease, osteoarthritis, osteoporosis, Alzheimer's disease, cataracts, and others.
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3. Wikipedia: Wiskott-Aldrich syndrome
WikipediaLead section, transmission-route statement
Quote, Lead section, transmission-route statement
The WAS-related disorders of X-linked thrombocytopenia (XLT) and X-linked congenital neutropenia (XLN) may present with similar but less severe symptoms and are caused by mutations of the same gene.
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4. Wiskott-Aldrich Syndrome (Wikipedia)
Clinical syndrome described by Robert Aldrich in 1954View the Source
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