Allogeneic stem cell transplantation-A curative treatment for paroxysmal nocturnal hemoglobinuria with PIGT mutation: A case report

BACKGROUND: Patients with paroxysmal nocturnal hemoglobinuria (PNH) have a clonal population of blood cells deficient in glycosylphosphatidylinositol-anchored (GPI-anchored) proteins, most of the time resulting from a mutation in the X-linked gene PIGA. We report a patient with PNH resulting from a...

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Detalles Bibliográficos
Autores principales: Schenone, Laurence, Notarantonio, Anne-Béatrice, Latger-Cannard, Véronique, Fremeaux-Bacchi, Veronique, De Carvalho-Bittencourt, Marcelo, Rubio, Marie-Thérèse, Muller, Marc, D'Aveni, Maud
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9258387/
https://www.ncbi.nlm.nih.gov/pubmed/35979111
http://dx.doi.org/10.12998/wjcc.v10.i17.5702

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9258387/
https://www.ncbi.nlm.nih.gov/pubmed/35979111
http://dx.doi.org/10.12998/wjcc.v10.i17.5702

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