Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

SDHC phaeochromocytoma and paraganglioma: A UK‐wide case series

24 Sept 2021

Abstract excerpt

OBJECTIVE: Phaeochromocytomas and paragangliomas (PPGL) are rare, but strongly heritable tumours. Variants in succinate dehydrogenase (SDH) subunits are identified in approximately 25% of cases. However, clinical and genetic information of patients with SDHC variants are underreported. DESIGN: This retrospective case series collated data from 18 UK Genetics and Endocrinology departments. PATIENTS: Both...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Adrenal and Paraganglionic Tumors
Share to Cancer, Hypoxia, and Metabolism
Share to Pituitary Gland Disorders and Treatments

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 34558728
DOI: 10.1111/cen.14594

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

SDHC phaeochromocytoma and paraganglioma: A UK‐wide case seriesPMID 34558728Read ↗

Pathology and genetics of phaeochromocytoma and paragangliomaSemantic proximity Read ↗

SDH mutations in tumorigenesis and inherited endocrine tumours: lesson from the phaeochromocytoma-paraganglioma syndromes.Semantic proximity Read ↗

The Changing Paradigm of Head and Neck Paragangliomas: What Every Otolaryngologist Needs to Know.Semantic proximity Read ↗

15 YEARS OF PARAGANGLIOMA: Genetics and mechanism of pheochromocytoma–paraganglioma syndromes characterized by germline SDHB and SDHD mutationsSemantic proximity Read ↗

UK recommendations for SDHA germline genetic testing and surveillance in clinical practice.Semantic proximity Read ↗

Pheochromocytoma and paraganglioma syndromes: genetics and management updateSemantic proximity Read ↗

Evaluation of SDHB, SDHD and VHL gene susceptibility testing in the assessment of individuals with non-syndromic phaeochromocytoma, paraganglioma and head and neck paraganglioma.Semantic proximity Read ↗

Tumour risks and genotype-phenotype correlations associated with germline variants in succinate dehydrogenase subunit genes SDHB, SDHC and SDHD.Semantic proximity Read ↗

Variant type is associated with disease characteristics in SDHB, SDHC and SDHD-linked phaeochromocytoma–paragangliomaSemantic proximity Read ↗

New Insights on the Genetics of Pheochromocytoma and Paraganglioma and Its Clinical ImplicationsSemantic proximity Read ↗

Germline SDHB and SDHD mutations in pheochromocytoma and paraganglioma patientsSemantic proximity Read ↗

Clinical manifestations of familial paraganglioma and phaeochromocytomas in succinate dehydrogenase B (SDH-B) gene mutation carriers.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.