Wiskott-Aldrich Syndrome

Wiskott-Aldrich Syndrome (WAS) is a rare genetic condition primarily affecting males. It is characterized by three main features: eczema, recurrent infections due to immune deficiency, and an increased risk of bleeding due to low platelet levels. This syndrome is caused by mutations in the WAS gene, which is involved in immune system function. Symptoms typically appear in early childhood. Ongoing medical care is essential for managing infections and other complications, and treatments may include immunotherapy or bone marrow transplants to improve immune function and overall health.