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Article

Familial paraganglioma syndromes.

Journal of clinical pathology - 1 Jun 2010

Chetty Runjan

Abstract excerpt

Paragangliomas and phaeochromocytomas may occur in syndromic or sporadic forms. The former are well recognised with multiple endocrine neoplasia (MEN) type 2 and von Hippel-Lindau syndromes. A few cases are associated with neurofibromatosis type 1. The familial paraganglioma-phaeochromocytoma syndromes are less well recognised, but as more genetic testing is performed, more cases belonging to this syndrome will...

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Source

Identifiers

PMID: 20498024
DOI: 10.1136/jcp.2010.076257

Genes

SDHC
SDHD
SDHB

Provenance

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