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Hereditary Paraganglioma-Pheochromocytoma Syndrome

Known as: Familial Paraganglioma-Pheochromocytoma Syndrome 
An autosomal dominant hereditary syndrome caused by mutations in the SDHD, SDHC, SDHB, and SDHAF2 genes. It is characterized by the development of… 
National Institutes of Health

Related topics

Related topics

8 relations
Endocrine systemParagangliomaSDHB geneSDHB wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Tumor detection rates in screening carriers with SDHx-related hereditary paraganglioma-pheochromocytoma syndrome based on prior tumor history.
1545Background: Patients with germline pathogenic variants (PVs) in the SDHx genes have increased risk for paragangliomas… 
Review
2019
Review
2019
Paraganglioma of the Vagina Associated With Germline SDHB Mutation: Report of a Case With Review of the Literature.
Paragangliomas are rare neuroendocrine neoplasms in the vagina, and their molecular pathogenesis has not been documented. We… 
2017
2017
The Hereditary Paraganglioma-Pheochromocytoma Syndrome: No Time to Waste.
2016
2016
Combined Treatment With 131I-MIBG and Sunitinib Induces Remission in a Patient With Metastatic Paraganglioma Due to Hereditary Paraganglioma-Pheochromocytoma Syndrome From an SDHB Mutation.
A 22-year-old woman with rapidly progressing metastatic paraganglioma due to hereditary paraganglioma-pheochromocytoma syndrome… 
Review
2012
Review
2012
Necessity for long-term follow-up of patients with head and neck paraganglioma and mutation in the succinate dehydrogenase genes: an index case report and literature review.
OBJECTIVE To describe a patient with hereditary head and neck paraganglioma (HNPGL) and to review the literature on these rare… 
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