Werner's Syndrome: Understanding the Phenotype of Premature Aging—First Case Described in Colombia

Werner's syndrome (WS) is an autosomal recessive genetic disease, which is mainly characterized by scleroderma-like skin changes, juvenile cataracts, short stature, and signs of premature aging. We report a case of a 48-year-old male patient, who presents with cardinal signs of WS including hig...

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Detalles Bibliográficos
Autores principales: Rincón, A., Mora, L., Suarez-Obando, F., Rojas, J. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6390251/
https://www.ncbi.nlm.nih.gov/pubmed/30891318
http://dx.doi.org/10.1155/2019/8538325

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6390251/
https://www.ncbi.nlm.nih.gov/pubmed/30891318
http://dx.doi.org/10.1155/2019/8538325

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