Wiscott-Aldrich syndrome (WAS)

Ghafari, J and Karami, H and Khanian, A.A and SoleimaniRad, H (2009) Wiscott-Aldrich syndrome (WAS). Journal of Mazandaran University of Medical Sciences, 19 (70). pp. 85-90.

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Official URL: http://jmums.mazums.ac.ir/article-1-556-en.html

Abstract

Wiscott-Aldrich syndrome (WAS) is an x-linked immune-deficiency disorder associated with eczema, recurrent infections, and increased frequency of autoimmune diseases, malignancy and thrombocytopenia with small size platelet. Our case is an 11 year old from a non- related parent, who was admitted with abdominal pain (hematoma), lower extremities bleeding (ecchymosed) and vomiting. Also, he had many admit ion cause bleeding in different areas. Lastly, he had retinal bleeding associated with blindness from 1 year ago.

Item Type: Article
Uncontrolled Keywords: Wiscott-Aldrich syndrome, immunodeficiency, blindness
Depositing User: Unnamed user with email eprints@mazums.ac.ir
Date Deposited: 04 Jan 2018 17:41
Last Modified: 04 Jan 2018 17:41
URI: http://eprints.mazums.ac.ir/id/eprint/3385

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