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Mutations associated with succinate dehydrogenase D-related malignant paragangliomas.
- Source :
- Clinical Endocrinology; 561; 566; 0300-0664; 4; 68; ~Clinical Endocrinology~561~566~~~0300-0664~4~68~~
- Publication Year :
- 2008
-
Abstract
- Contains fulltext : 70804.pdf (publisher's version ) (Closed access)<br />OBJECTIVE: Hereditary paraganglioma (PGL) syndromes result from germline mutations in genes encoding subunits B, C and D of the mitochondrial enzyme succinate dehydrogenase (SDHB, SDHC and SDHD). SDHB-related PGLs are known in particular for their high malignant potential. Recently, however, malignant PGLs were also reported among a small minority of Dutch carriers of the SDHD founder mutation D92Y. The aim of the study was to investigate which SDHD mutations are associated with malignant PGL. DESIGN: Case histories; collaborative study between referral centres in France, the USA, and the Netherlands. PATIENTS: Six unrelated patients with metastatic PGLs of either sympathetic or parasympathetic origin. MEASUREMENTS: Assessment of SDHD mutations underlying malignant PGL. RESULTS: Germline SDHD mutations underlying metastatic PGL were G148D, Y114X, L85X, W43X, D92Y, and IVS2+5G-->A. CONCLUSION: Our findings indicate that malignant SDHD-related PGL is associated with several mutations besides D92Y.
Details
- Database :
- OAIster
- Journal :
- Clinical Endocrinology; 561; 566; 0300-0664; 4; 68; ~Clinical Endocrinology~561~566~~~0300-0664~4~68~~
- Publication Type :
- Electronic Resource
- Accession number :
- edsoai.on1284106922
- Document Type :
- Electronic Resource