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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| 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
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| Series: | The Turkish Journal of Pediatrics |
| Online Access: | https://turkjpediatr.org/article/view/2598 |
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