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New Insights on the Genetics of Pheochromocytoma and Paraganglioma and Its Clinical Implications

New Insights on the Genetics of Pheochromocytoma and Paraganglioma and Its Clinical Implications

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8833412

New Insights on the Genetics of Pheochromocytoma and Paraganglioma and Its Clinical Implications

About this item

Full title

New Insights on the Genetics of Pheochromocytoma and Paraganglioma and Its Clinical Implications

Publisher

Switzerland: MDPI AG

Journal title

Cancers, 2022-01, Vol.14 (3), p.594

Language

English

Formats

Publication information

Publisher

Switzerland: MDPI AG

More information

Scope and Contents

Contents

Pheochromocytomas (PHEOs) and paragangliomas (PGLs) are rare neuroendocrine tumors that arise from chromaffin cells. PHEOs arise from the adrenal medulla, whereas PGLs arise from the neural crest localized outside the adrenal gland. Approximately 40% of all cases of PPGLs (pheochromocytomas/paragangliomas) are associated with germline mutations and...

Alternative Titles

Full title

New Insights on the Genetics of Pheochromocytoma and Paraganglioma and Its Clinical Implications

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8833412

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8833412

Other Identifiers

ISSN

2072-6694

E-ISSN

2072-6694

DOI

10.3390/cancers14030594

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