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Published in: High Blood Pressure & Cardiovascular Prevention 3/2008

01-07-2008 | Contributions from International Congress

6.3 Pheochromocytoma: Clinical, Diagnostic and Genetic Aspects: Experience in a Single Centre

Authors: D. Cotesta, L. Petramala, G. De Toma, A. Verrienti, S. Filetti, C. Letizia

Published in: High Blood Pressure & Cardiovascular Prevention | Issue 3/2008

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Excerpt

Introduction. Pheochromocytomas and paragangliomas are rare tumours with common embriogenetic origin, pheochromocytoma can be sporadic or syndromic. There are four different syndromes genetically determined (MEN 2, paraganglioma/pheochromocytoma syndrome, Von Hippel Lindau syndrome and neurofibromatosis type 1). …
Metadata
Title
6.3 Pheochromocytoma: Clinical, Diagnostic and Genetic Aspects: Experience in a Single Centre
Authors
D. Cotesta
L. Petramala
G. De Toma
A. Verrienti
S. Filetti
C. Letizia
Publication date
01-07-2008
Publisher
Springer International Publishing
Published in
High Blood Pressure & Cardiovascular Prevention / Issue 3/2008
Print ISSN: 1120-9879
Electronic ISSN: 1179-1985
DOI
https://doi.org/10.1007/BF03263650

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