A mutation of the succinate dehydrogenase B gene in a Korean family with paraganglioma

Fam Cancer. 2016 Oct;15(4):601-6. doi: 10.1007/s10689-016-9874-8.

Abstract

Familial paraganglioma (PGL) is a dominantly inherited disorder characterized by development of PGLs in the head and neck region. Germline mutations in genes coding for succinate dehydrogenase (SDH) subunits D, B, and C (SDHD, SDHB, SDHC) are found in almost all familial PGL patients. A 19-year-old female presented with pulsatile tinnitus and a reddish pulsating mass in the external auditory canal, and her mother complained of similar symptoms. Paraganglioma was found in both patients and was surgically removed. We report a case of germline SDHB mutation. This mutation was a deletion of thymine at nucleotide position 757 in exon 7 of the SDHB gene (c.757delT).

Keywords: Germ-line mutation; Paraganglioma; Succinate dehydrogenase.

Publication types

  • Case Reports

MeSH terms

  • Asian People / genetics
  • Ear Neoplasms / genetics
  • Ear Neoplasms / surgery
  • Female
  • Germ-Line Mutation*
  • Heterozygote
  • Humans
  • Paraganglioma / genetics*
  • Paraganglioma / surgery
  • Succinate Dehydrogenase / genetics*
  • Tinnitus / genetics
  • Tinnitus / pathology
  • Tympanic Membrane / pathology
  • Young Adult

Substances

  • SDHB protein, human
  • Succinate Dehydrogenase