Acquired spherocytosis in the setting of myelodysplasia

Hereditary spherocytosis (HS) is the most prevalent red blood cell (RBC) membrane disorder. We report a rare case of acquired SPTB spherocytosis coinciding with a myelodysplastic syndrome associated U2AF1 mutation, neither found in germline DNA. The diagnosis was confirmed by Eosin-5-Maleimide bindi...

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Detalles Bibliográficos
Autores principales: Karlsson, Linda Katharina, Mottelson, Mathis Nygaard, Helby, Jens, Petersen, Jesper, Glenthøj, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9198317/
https://www.ncbi.nlm.nih.gov/pubmed/35720514
http://dx.doi.org/10.1016/j.lrr.2022.100332

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9198317/
https://www.ncbi.nlm.nih.gov/pubmed/35720514
http://dx.doi.org/10.1016/j.lrr.2022.100332

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