Optimizing Genetic Workup in Pheochromocytoma and Paraganglioma by Integrating Diagnostic and Research Approaches

Optimizing Genetic Workup in Pheochromocytoma and Paraganglioma by Integrating Diagnostic and Research Approaches

Pheochromocytomas and paragangliomas (PPGL) are rare neuroendocrine tumors with a strong hereditary background and a large genetic heterogeneity. Identification of the underlying genetic cause is crucial for the management of patients and their families as it aids differentiation between hereditary...

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Bibliographic Details
Main Authors: Laura Gieldon, Doreen William, Karl Hackmann, Winnie Jahn, Arne Jahn, Johannes Wagner, Andreas Rump, Nicole Bechmann, Svenja Nölting, Thomas Knösel, Volker Gudziol, Georgiana Constantinescu, Jimmy Masjkur, Felix Beuschlein, Henri JLM Timmers, Letizia Canu, Karel Pacak, Mercedes Robledo, Daniela Aust, Evelin Schröck, Graeme Eisenhofer, Susan Richter, Barbara Klink
Format: Article
Language:English
Published: MDPI AG 2019-06-01
Series:Cancers
Subjects:
pheochromocytoma
paraganglioma
next-generation sequencing
sporadic
hereditary
CNV detection
Online Access:https://www.mdpi.com/2072-6694/11/6/809

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https://www.mdpi.com/2072-6694/11/6/809

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