Inherited Human BCL10 Deficiencies.
Ashwag A AlsaidalaniBlanca García-SolísEsraa BukhariAna Van Den RymEduardo López-CollazoSilvia Sánchez-RamónFernando CorvilloAlberto López-LeraAna de AndrésRubén Martínez-BarricarteRebeca Perez de DiegoPublished in: Journal of clinical immunology (2023)
Human BCL10 deficiency causes combined immunodeficiency with bone marrow transplantation as its only curative option. To date, there are four homozygous mutations described in the literature that were identified in four unrelated patients. Here, we describe a fifth patient with a novel mutation and summarize what we have learned about BCL10 deficiency. Due to the severity of the disease, accurate knowledge of its clinical and immunological characteristics is instrumental for early diagnosis and adequate clinical management of the patients.