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Any dyskeratosis congenita in which the cause of the disease is a mutation in the DKC1 gene.
No clinical trials have been registered for DKC1-related disorder.
5 publications have been identified in PubMed for DKC1-related disorder. Research spans Basic Science / Preclinical (60%), Case Report / Case Series (20%), and Epidemiology / Natural History (20%).
Haghipanah M (2026). [PMID: 41547964](https://pubmed.ncbi.nlm.nih.gov/41547964/). *Pediatr Res*. [Epidemiology / Natural History]
Kasapoğlu H (2026). [PMID: 42256974](https://pubmed.ncbi.nlm.nih.gov/42256974/). *Clin Case Rep*. [Case Report / Case Series]
Valeeva EV (2025). [PMID: 40272729](https://pubmed.ncbi.nlm.nih.gov/40272729/). *J Mol Neurosci*. [Basic Science / Preclinical]
Wang CY (2024). [PMID: 39256642](https://pubmed.ncbi.nlm.nih.gov/39256642/). *Mol Med*. [Basic Science / Preclinical]
Chang CH (2024). [PMID: 39326821](https://pubmed.ncbi.nlm.nih.gov/39326821/). *Exp Neurol*. [Basic Science / Preclinical]
Data assembled from 2 of 12 sources · Last updated Sep 19, 2026, 11:50 PM UTC
Common questions about DKC1-related disorder