A case of Wiskott-Aldrich syndrome with de novo mutation at exon 4

Wiskott-Aldrich syndrome (WAS) is an X-linked disorder characterized by thrombocytopenia, eczema and immunodeficiency. Clinical features of the disease are highly varied; therefore, the diagnosis is sometimes difficult, especially in solitary cases or cases with milder forms of the disease. H...

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Bibliographic Details
Main Authors: Figen Doğu, Tadashi Ariga, Aydan Ikincioğullari, Günseli Bozdoğan, Caner Aytekin, Ayşe Metin, Emel Babacan
Format: Article
Language:English
Published: Hacettepe University Institute of Child Health 2006-01-01
Series:The Turkish Journal of Pediatrics
Online Access:https://turkjpediatr.org/article/view/2598
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