Case Report: A novel WRN mutation in Werner syndrome patient with diabetic foot disease and myelodysplastic syndrome

Werner syndrome is an autosomal recessive rare disease caused by a WRN gene mutation, which is rarely reported in the Chinese population. We report the clinical and genetic data of a Chinese patient with Werner syndrome. The proband was a 40-year-old male patient who presented with diabetic foot ulc...

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Detalles Bibliográficos
Autores principales: Peng, Huifang, Wang, Jie, Liu, Yanyun, Yang, Haiping, Li, Liping, Ma, Yujin, Zhuo, Huiqin, Jiang, Hongwei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9334726/
https://www.ncbi.nlm.nih.gov/pubmed/35909544
http://dx.doi.org/10.3389/fendo.2022.918979

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9334726/
https://www.ncbi.nlm.nih.gov/pubmed/35909544
http://dx.doi.org/10.3389/fendo.2022.918979

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