The clinical genetics of phaeochromocytoma and paraganglioma

ABSTRACT Phaeochromocytoma and paraganglioma are rare catecholamine-producing tumours, recognised to have one of the richest hereditary backgrounds of all neoplasms, with germline mutations seen in approximately 30% of patients. They can be a part of genetic syndromes such as MEN 2 or Neurofibromato...

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Autors principals: P. T. Kavinga Gunawardane, Ashley Grossman
Format: Article
Idioma:English
Publicat: Brazilian Society of Endocrinology and Metabolism
Col·lecció:Archives of Endocrinology and Metabolism
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Accés en línia:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S2359-39972017000500490&lng=en&tlng=en