International Journal of Science and Research (IJSR)
Since Year 2012 | Open Access | Fully Refereed | Peer Reviewed

Downloads: 91

Case Studies | Nursing | India | Volume 9 Issue 9, September 2020

Wiskott Aldrich Syndrome - A Case Report

Latha Gracelin P. ^[3] | Amalorpavamari Lucas ^[6]

Abstract: Wiskott Aldrich Syndrome (WAS) is an immunological disorder caused by a genetic abnormality (Brunner, 2017). WAS is a rare genetic disorder of the immune system that primarily affects boys. It is characterized by abnormal immune function and a reduced ability to form blood clots. It is one of the primary immune deficiency disorders (NIAID, 2015) which results in prolonged bleeding and recurrent infections. The platelet abnormality is typically present from birth and can lead to easy bruising or episodes of prolonged bleeding following minor trauma. Early correction with hematopoietic stem cell transplantation or gene therapy is necessary to prevent the risk of Severe Combined Immunodeficiency (SCID), autoimmune complications and Haematological malignancies. This article glimpses a case scenario with WAS disease and the medical and nursing management carried out in a tertiary care hospital in southern India which is one of the pioneer hospitals for Haematopoietic stem cell transplantation in India.

Keywords: genetic, bleeding, infection, hematopoietic stem cell transplantation

Edition: Volume 9 Issue 9, September 2020,

Pages: 566 - 573

Wiskott Aldrich Syndrome - A Case Report

How to Cite this Article?

Latha Gracelin P., Amalorpavamari Lucas, "Wiskott Aldrich Syndrome - A Case Report", International Journal of Science and Research (IJSR), https://www.ijsr.net/get_abstract.php?paper_id=SR20903153718, Volume 9 Issue 9, September 2020, 566 - 573, #ijsrnet

How to Share this Article?

Similar Articles with Keyword 'genetic'