Pulmonary fibrosis in dyskeratosis congenita: a case report with a PRISMA-compliant systematic review

BACKGROUND: Dyskeratosis congenita (DC) is a rare genetic disorder of poor telomere maintenance. Pulmonary fibrosis (PF) related to DC is rarely reported. CASE PRESENTATION: A 23-year-old student presented with a four-year history of progressive cough and exertional dyspnea. Physical examination was...

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Detalles Bibliográficos
Autores principales: Wang, Ping, Xu, Zuojun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8418029/
https://www.ncbi.nlm.nih.gov/pubmed/34479523
http://dx.doi.org/10.1186/s12890-021-01645-w

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8418029/
https://www.ncbi.nlm.nih.gov/pubmed/34479523
http://dx.doi.org/10.1186/s12890-021-01645-w

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