Cargando…
Cernunnos defect in an Iranian patient with T(−) B(+) NK (+) severe combined immunodeficiency: A case report and review of the literature
BACKGROUND: Defective Cernunnos gene in nonhomologous end‐joining (NHEJ) pathway of the DNA repair is responsible for radiosensitive severe combined immunodeficiency (SCID). Herein, presented a new patient with Cernunnos deficiency and summarized the clinical, immunological, and molecular features o...
Autores principales: | Jamee, Mahnaz, Khakbazan Fard, Nasrin, Fallah, Shahrzad, Golchehre, Zahra, Fallahi, Mazdak, Shamsian, Bibi Shahin, Sharafian, Samin, Chavoshzadeh, Zahra |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9356558/ https://www.ncbi.nlm.nih.gov/pubmed/35656589 http://dx.doi.org/10.1002/mgg3.1990 |
Ejemplares similares
-
A rare immunological disease, caspase 8 deficiency: case report and literature review
por: Bazgir, Narges, et al.
Publicado: (2023) -
Demographic, clinical, immunological, and molecular features of iranian national cohort of patients with defect in DCLRE1C gene
por: Ghadimi, Soodeh, et al.
Publicado: (2023) -
Novel PGM3 mutation in two siblings with combined immunodeficiency and childhood bullous pemphigoid: a case report and review of the literature
por: Fallahi, Mazdak, et al.
Publicado: (2022) -
JAGN1 mutation with distinct clinical features; two case reports and literature review
por: Hojabri, Mahsa, et al.
Publicado: (2023) -
Immunodeficiency due to a novel variant in PIK3CD: a case report
por: Shashaani, Niloofar, et al.
Publicado: (2023)