The Misleading Normal in an Unusual Case of Wiskott–Aldrich Syndrome: A Case Report with Review of Literature

Wiskott–Aldrich syndrome (WAS) is a rare X-linked disorder characterized by thrombocytopenia, eczema, and immunodeficiency. Mutations in the WAS gene disrupt hematopoietic cell actin cytoskeletal reorganization, often leading to classic small platelets, although variants exist. We present the case o...

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Bibliographic Details
Main Authors: Vanya Rai, Saurav Sharma, Amitabh Singh, Sumit Mehndiratta, Nidhi Chopra
Format: Article
Language:English
Published: Thieme Medical and Scientific Publishers Pvt. Ltd.
Series:Indian Journal of Medical and Paediatric Oncology
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Online Access:http://www.thieme-connect.de/DOI/DOI?10.1055/s-0045-1805089
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