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- W2337371683 abstract "The prevalence of pheochromcytoma in hypertensive patients is less than 1%.Most PHEOs occur sporadically, but a substantial proportionmay be associated with germ line mutations of genes predisposing to thedevelopment of familial syndromes like multiple endocrineneoplasia(MEN),Von-Hippel Lindau(VHL) disease,neurofibromatosis type 1(NF-1),familial paraganglioma/pheochromocytoma (PGL/PHEO) related to geneticmutation encoding the mitochondrial protein succinate dehdrogenase sub units(SDH-BCD) .Screening for genetic mutation is imperative as it may add more onmanagement and surveillance of this patients .This review summarize therelevant data related to this fascinating clinical entity." @default.
- W2337371683 created "2016-06-24" @default.
- W2337371683 creator A5052800559 @default.
- W2337371683 date "2013-11-30" @default.
- W2337371683 modified "2023-09-27" @default.
- W2337371683 title "Genetic Pheochromocytoma -a Review" @default.
- W2337371683 doi "https://doi.org/10.14196/sjms.v2i11.1023" @default.
- W2337371683 hasPublicationYear "2013" @default.
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