Cowden Disease: Case Report and Review of the Literature

Cowden's disease is a rare autosomal dominant, multiple hamartoma syndrome with characteristic mucocutaneous lesions. It is associated with abnormalities of the breast, thyroid, and gastrointestinal tract; and is characterized by multiple hamartomas in the gastrointestinal tract and mucocutaneo...

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Detalles Bibliográficos
Autores principales: Son, Jee Hee, Chung, Bo Young, Jung, Min Je, Choi, Yong Won, Kim, Hye One, Park, Chun Wook
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Dermatological Association; The Korean Society for Investigative Dermatology 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7992722/
https://www.ncbi.nlm.nih.gov/pubmed/33911599
http://dx.doi.org/10.5021/ad.2019.31.3.325

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7992722/
https://www.ncbi.nlm.nih.gov/pubmed/33911599
http://dx.doi.org/10.5021/ad.2019.31.3.325

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