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The Wiskott-Aldrich Foundation is a non-profit organization dedicated to funding research to find improved cures for WAS ,providing up-to-date information and support for families living with Wiskott-Aldrich Syndrome worldwide.
https://ghr.nlm.nih.gov/condition/wiskott-aldrich-syndrome
Oct 29, 2019 · Wiskott-Aldrich syndrome is characterized by abnormal immune system function (immune deficiency), eczema (an inflammatory skin disorder characterized by abnormal patches of red, irritated skin), and a reduced ability to form blood clots. This condition primarily affects males.
https://rarediseases.info.nih.gov/diseases/7895/wiskott-aldrich-syndrome
74 rows · Dec 05, 2017 · Wiskott Aldrich syndrome (WAS) is a disease with immunological …
https://www.niaid.nih.gov/sites/default/files/Wiskott-Aldrich-Syndrome-Factsheet.pdf
stress of any illness is controllable and an important aspect of managing Wiskott-Aldrich syndrome. Children also learn who they can turn to for support and how to solve problems. Acknowledging both the challenges and opportunities that Wiskott-Aldrich syndrome presents helps children develop resilience.
http://www.wiskott.org/about-us
The Wiskott-Aldrich Foundation was created with the mission to provide information, enable research, and provide support for WAS families worldwide. The foundation has been serving families with WAS since 2003 as the For Pete’s Sake Foundation, which was the first organized charitable support for families with WAS.
https://www.ncbi.nlm.nih.gov/books/NBK539838/
Wiskott-Aldrich syndrome is a rare X-linked disorder with a characteristic triad of immunodeficiency, thrombocytopenia, and eczema. It results from a genetic mutation in the gene encoding Wiskott-Aldrich syndrome protein (WASp) affecting the immune system and inducing a state of immunodeficiency.Author: Muhammad Ahmed Malik, Muhammad Masab
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