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The patient was found to have a mutation in the succinyl dehydrogenase B (SDHB) gene, which is causative for SDHB-related hereditary paraganglioma-pheochromocytoma syndrome. Herein, we describe her presentation and medical management and discuss the clinical implications of SDHB deficiency.<\/jats:p>","DOI":"10.1155\/2014\/273423","type":"journal-article","created":{"date-parts":[[2014,8,19]],"date-time":"2014-08-19T17:10:47Z","timestamp":1408468247000},"page":"1-7","source":"Crossref","is-referenced-by-count":0,"title":["Pheochromocytoma in a Twelve-Year-Old Girl with SDHB-Related Hereditary Paraganglioma-Pheochromocytoma Syndrome"],"prefix":"10.1155","volume":"2014","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-9887-6267","authenticated-orcid":true,"given":"Daryl","family":"Graham","sequence":"first","affiliation":[{"name":"Department of Pediatrics, University of Kentucky College of Medicine, Lexington, KY 40536, USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Megan","family":"Gooch","sequence":"additional","affiliation":[{"name":"University of Kentucky College of Medicine, Lexington, KY 40536, 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