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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Detalhes bibliográficos
Publicado no:Ann Dermatol
Main Authors: Son, Jee Hee, Chung, Bo Young, Jung, Min Je, Choi, Yong Won, Kim, Hye One, Park, Chun Wook
Formato: Artigo
Idioma:Inglês
Publicado em: The Korean Dermatological Association; The Korean Society for Investigative Dermatology 2019
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7992722/
https://ncbi.nlm.nih.gov/pubmed/33911599
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5021/ad.2019.31.3.325
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