Cargando…
When WAS Gene Diagnosis Is Needed: Seeking Clues Through Comparison Between Patients With Wiskott-Aldrich Syndrome and Idiopathic Thrombocytopenic Purpura
Background: Wiskott-Aldrich syndrome (WAS) is a rare and severe X-linked disorder with variable clinical phenotypes correlating with the type of mutations in the WAS gene. The syndrome is difficult to differentiate from idiopathic thrombocytopenic purpura (ITP) before genetic diagnosis. We retrospec...
Autores principales: | Jin, Ying-Ying, Wu, Jing, Chen, Tong-Xin, Chen, Ji |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6634258/ https://www.ncbi.nlm.nih.gov/pubmed/31354712 http://dx.doi.org/10.3389/fimmu.2019.01549 |
Ejemplares similares
-
Wiskott–Aldrich syndrome that was initially diagnosed as immune thrombocytopenic purpura secondary to a cytomegalovirus infection
por: Kaneko, Ryota, et al.
Publicado: (2018) -
Unraveling the Repertoire in Wiskott–Aldrich Syndrome
por: Petersen, Sven H., et al.
Publicado: (2014) -
Autoimmunity in Wiskott–Aldrich Syndrome: An Unsolved Enigma
por: Catucci, Marco, et al.
Publicado: (2012) -
Síndrome de Wiskott - Aldrich /
por: Tello Gabriel, Adriana -
Wiskott Aldrich Syndrome: A Multi-Institutional Experience From India
por: Suri, Deepti, et al.
Publicado: (2021)