Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.12530/54591
Title: Considerations on diagnosis and surveillance measures of PTEN hamartoma tumor syndrome: clinical and genetic study in a series of Spanish patients
Authors: 
Filiation: Servicio de Oncología Médica. Hospital Universitario de Fuenlabrada
Servicio de Dermatología. Hospital Universitario de Fuenlabrada
Keywords: 
Mesh: Hamartoma Syndrome, Multiple
Decs: 
Issue Date: 28-Feb-2022
Citation: Pena-Couso L, Ercibengoa M, Mercadillo F, Gómez-Sánchez D, Inglada-Pérez L, Santos M, et al. Considerations on diagnosis and surveillance measures of PTEN hamartoma tumor syndrome: clinical and genetic study in a series of Spanish patients. Orphanet Journal of Rare Diseases. 2022;17(1):85.
Abstract: The limited knowledge about the PTEN hamartoma tumor syndrome (PHTS) makes its diagnosis a challenging task. We aimed to define the clinical and genetic characteristics of this syndrome in the Spanish population and to identify new genes potentially associated with the disease.
PMID: 35227301
URI: https://hdl.handle.net/20.500.12530/54591
Rights: info:eu-repo/semantics/openAccess
Appears in Collections:Hospitales > H. U. de Fuenlabrada > Artículos

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