Blau syndrome with persistent fetal vasculature: a case report

BACKGROUND: Blau Syndrome (BS) is a rare autosomal dominant noncaseous granulomatous disease caused by mutations in the NOD2 gene. The disease is characterized by granulomatous dermatitis, symmetrical arthritis, and uveitis, which, if left untreated, can progress to blindness. The diagnosis of BS ca...

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Detalles Bibliográficos
Autores principales: Liu, Miao, Zeng, Yong, Zhong, Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10311772/
https://www.ncbi.nlm.nih.gov/pubmed/37386644
http://dx.doi.org/10.1186/s13256-023-03983-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10311772/
https://www.ncbi.nlm.nih.gov/pubmed/37386644
http://dx.doi.org/10.1186/s13256-023-03983-1

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