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CASE REPORT: FAMILIAL WISKOTT-ALDRICH SYNDROME

Wiskott-Aldrich syndrome (WAS) is a rare X-linked recessive disorder characterized by a triad of symptoms: immunodeficiency, thrombocytopenia, and eczema. It arises from a mutation in the gene encoding the WAS protein (WASp). The disease can present with varying degrees of severity, ranging from cla...

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Uloženo v:
Hlavní autoři: Belykh Natalia Anatolievna, Glotova Inna Aleksandrovna, Deeva Yuliya Vitalievna, Piznyur Inna Vladimirovna
Médium: Artigo
Jazyk:Inglês
Vydáno: Avicenna Tajik State Medical University 2024-12-01
Edice:Паёми Сино
Témata:
children
immunodeficiency
wiskott-aldrich syndrome
thrombocytopenia
hematopoietic stem cell transplantation
clinical case.
On-line přístup:https://doi.org/10.25005/2074-0581-2024-26-4-700-709
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