Dyskeratosis congenita: natural history of the disease through the study of a cohort of patients diagnosed in childhood
BackgroundDyskeratosis congenita (DC) is a multisystem and ultra-rare hereditary disease characterized by somatic involvement, bone marrow failure, and predisposition to cancer. The main objective of this study is to describe the natural history of DC through a cohort of patients diagnosed in childh...
Main Authors: | M. L. Uria-Oficialdegui, S. Navarro, L. Murillo-Sanjuan, C. Rodriguez-Vigil, M. I. Benitez-Carbante, C. Blazquez-Goñi, J. A. Salinas, C. Diaz-de-Heredia |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2023-08-01
|
Series: | Frontiers in Pediatrics |
Subjects: | |
Online Access: | https://www.frontiersin.org/articles/10.3389/fped.2023.1182476/full |
Similar Items
-
Dyskeratosis Congenita and Short Telomeres in a Female Patient
by: Virgínia Vinha Zanuncio, et al.
Published: (2020-12-01) -
The evolving genetic landscape of telomere biology disorder dyskeratosis congenita
by: Hemanth Tummala, et al.
Published: (2024-08-01) -
Severe immunochemotherapy-induced toxicities in a patient with dyskeratosis congenita and literature review
by: Jiayi Geng, et al.
Published: (2022-12-01) -
Case report: A novel mutation in RTEL1 gene in dyskeratosis congenita
by: Haider Nisar, et al.
Published: (2023-03-01) -
Punctal and Canalicular Obstruction Associated with Dyskeratosis Congenita
by: Taner Kar, et al.
Published: (2015-01-01)