Mutations associated with succinate dehydrogenase d-related malignant paragangliomas
Research output: Contribution to journal › Research article › Contributed › peer-review
Contributors
Abstract
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
Original language | English |
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Pages (from-to) | 561-566 |
Number of pages | 6 |
Journal | Clinical endocrinology |
Volume | 68 |
Issue number | 4 |
Publication status | Published - Apr 2008 |
Peer-reviewed | Yes |
Externally published | Yes |
External IDs
PubMed | 17973943 |
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