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Case Report: Identification of a Novel Pathogenic Germline TP53 Variant in a Family With Li-Fraumeni Syndrome.
Paduano, Francesco; Fabiani, Fernanda; Colao, Emma; Trapasso, Francesco; Perrotti, Nicola; Barbieri, Vito; Baudi, Francesco; Iuliano, Rodolfo.
Afiliación
  • Paduano F; Medical Genetics Unit, University "Magna Graecia", Catanzaro, Italy.
  • Fabiani F; Department of Health Sciences, University "Magna Graecia", Catanzaro, Italy.
  • Colao E; Tecnologica Research Institute and Marrelli Health, Biomedical Section, Stem Cells and Medical Genetics Units, Crotone, Italy.
  • Trapasso F; Medical Genetics Unit, University "Magna Graecia", Catanzaro, Italy.
  • Perrotti N; Medical Genetics Unit, University "Magna Graecia", Catanzaro, Italy.
  • Barbieri V; Medical Genetics Unit, University "Magna Graecia", Catanzaro, Italy.
  • Baudi F; Department of Experimental and Clinical Medicine, University Magna Graecia of Catanzaro, Catanzaro, Italy.
  • Iuliano R; Medical Genetics Unit, University "Magna Graecia", Catanzaro, Italy.
Front Genet ; 12: 734809, 2021.
Article en En | MEDLINE | ID: mdl-34539758
Li-Fraumeni syndrome (LFS) is an inherited autosomal dominant disease characterized by a predisposition to many cancers. Germline pathogenic variants in TP53 are primarily responsible for LFS. By performing a targeted sequencing panel in a proband with liver carcinoma having a deceased son affected by osteosarcoma, we found the novel heterozygous frameshift variant c.645del (p.Ser215Argfs*32) in the TP53 gene. This variant co-segregated with typical LFS cancers in the family pedigree, consistent with the pathogenicity of this novel and previously undescribed TP53 variant.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Revista: Front Genet Año: 2021 Tipo del documento: Article País de afiliación: Italia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Revista: Front Genet Año: 2021 Tipo del documento: Article País de afiliación: Italia