Cargando…
Relevance of Germline Mutation Screening in Both Familial and Sporadic Head and Neck Paraganglioma for Early Diagnosis and Clinical Management
Background: Head and neck paraganglioma (PGL) are benign tumors that can cause important direct or surgery induced morbidity. Almost all familial and 11–29% of sporadic PGL are caused by inactivating germline mutations in succinate dehydrogenase (SDH) genes. Our aim was to screen for such mutations...
Autores principales: | Hermsen, Mario A., Sevilla, María A., Llorente, José Luis, Weiss, Marjan M., Grimbergen, Anneliese, Allonca, Eva, Garcia-Inclán, Cristina, Balbín, Milagros, Suárez, Carlos |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
IOS Press
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4619289/ https://www.ncbi.nlm.nih.gov/pubmed/20208144 http://dx.doi.org/10.3233/CLO-2009-0498 |
Ejemplares similares
-
Mutation analysis of SDHB and SDHC: novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma
por: Bayley, Jean-Pierre, et al.
Publicado: (2006) -
Nationwide study of patients with head and neck paragangliomas carrying SDHB germline mutations
por: Rijken, J. A., et al.
Publicado: (2018) -
The first Dutch SDHB founder deletion in paraganglioma – pheochromocytoma patients
por: Bayley, Jean-Pierre, et al.
Publicado: (2009) -
Prevalence of Germline Mutations in Patients with Pheochromocytoma or Abdominal Paraganglioma and Sporadic Presentation: A Population-Based Study in Western Sweden
por: Muth, Andreas, et al.
Publicado: (2012) -
Multimodality imaging of paragangliomas of the head and neck
por: Thelen, Jarett, et al.
Publicado: (2019)