A novel RAD51 variant resulting in Fanconi anemia identified in an infant with multiple congenital anomalies

Fanconi anemia, FA, is a rare, multi‐system disease caused by pathogenic variants in DNA repair genes. We report a novel RAD51 variant in an infant with FA whose tracheobronchomalacia has not been described in FA. His severe presentation expands the phenotype of RAD51‐associated FA, reported only in...

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Detalles Bibliográficos
Autores principales: Geilmann, Shelby, Solstad, Rachel, Palmquist, Rachel, Flores Daboub, Josue, Botto, Lorenzo D., Grubb, Peter H., Bonkowsky, Josh L., Longo, Nicola, Malone Jenkins, Sabrina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9850852/
https://www.ncbi.nlm.nih.gov/pubmed/36698515
http://dx.doi.org/10.1002/ccr3.6810

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9850852/
https://www.ncbi.nlm.nih.gov/pubmed/36698515
http://dx.doi.org/10.1002/ccr3.6810

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