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THU533 Cowden Syndrome: A Rare Disease With A Lasting Impact

Disclosure: C.S. Hastings: None. S.A. Patrick: None. D. James: None. Introduction: Cowden Syndrome (CS) is a genetic condition caused by an autosomal dominant mutation in the phosphatase and tensin homolog (PTEN) tumor suppressor gene. The prevalence of CS is approximately one in 200,000 and onset i...

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Detalles Bibliográficos
Autores principales: Hastings, Camden S, Patrick, Stephanie A, James, Deirdre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10555341/
http://dx.doi.org/10.1210/jendso/bvad114.2160