Clinical and genetic analysis of 2 rare cases of Wiskott–Aldrich syndrome from Chinese minorities: Two case reports

RATIONALE: Wiskott–Aldrich syndrome (WAS) is a rare X-linked recessive disease characterized by thrombocytopenia, small platelets, eczema, immunodeficiency, and an increased risk of autoimmunity and malignancies. X-linked thrombocytopenia (XLT), the milder phenotype of WAS, is always limited to thro...

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Detalles Bibliográficos
Autores principales: Liu, Haifeng, Wang, Yanchun, Li, Yangfang, Tao, Lvyan, Zhang, Yu, He, Xiaoli, Zhou, Yuantao, Liu, Xiaoning, Wang, Yan, Li, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
3500
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8078428/
https://www.ncbi.nlm.nih.gov/pubmed/33879693
http://dx.doi.org/10.1097/MD.0000000000025527

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8078428/
https://www.ncbi.nlm.nih.gov/pubmed/33879693
http://dx.doi.org/10.1097/MD.0000000000025527

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