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      Rare Germline DICER1 Variants in Pediatric Patients With Cushing's Disease: What Is Their Role? 

      Martínez de la Piscina Martín, Idoia; Hernández Ramírez, Laura C.; Portillo, Nancy; Gómez Gila, Ana L.; Urrutia, Inés; Martínez Salazar, Rosa; García Castaño, Alejandro; Aguayo Calcena, Aníbal; Rica, Itxaso; Gaztambide Sáenz, María Sonia; Faucz, Fabio R.; Keil, Margaret F.; Lodish, Maya B.; Quezado, Martha; Pankratz, Nathan; Chittiboina, Prashant; Lane, John; Kay, Denise M.; Mills, James L.; Castaño González, Luis Antonio ORCID; Stratakis, Constantine A.; Spanish Corticotroph Adenomas Collaborative (Frontiers Media, 2020)
      Context: The DICER1 syndrome is a multiple neoplasia disorder caused by germline mutations in the DICER1 gene. In DICER1 patients, aggressive congenital pituitary tumors lead to neonatal Cushing's disease (CD). The role ...