OR22-02 PTEN Hamartoma Tumor Syndrome in Pediatrics: Triggers for Evaluation and the Value of Surveillance

Context: PTEN Hamartoma Tumor Syndrome (PHTS) comprises a collection of rare clinical disorders characterized by germline mutations in the tumor suppressor gene PTEN. Current guidelines recommend screening for thyroid tumors beginning in pediatric age at the time of PHTS diagnosis; however, the bene...

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Detalles Bibliográficos
Autores principales: Baran, Julia, Tsai, Steven, Singleton, Daniel, Isaza, Amber, Brodeur, Garrett, MacFarland, Suzanne, Zelley, Kristin, Mamula, Petar, Bauer, Andrew Jacob
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Pediatric Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7209534/
http://dx.doi.org/10.1210/jendso/bvaa046.859

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7209534/
http://dx.doi.org/10.1210/jendso/bvaa046.859

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