Literature DB >> 16080474

Carotid body paraganglioma and SDHD mutation in a Greek family.

C D Liapis1, J K Bellos, A Halapas, P Lembessis, M Koutsilieris, A Kostakis.   

Abstract

BACKGROUND: Carotid body (CB) is a highly specialized paraganglion originating from the neural crest ectoderm. CB paraganglion can be caused either by a genetic predisposition (hereditary paraganglia) or by chronic hypoxic stimulation. Germline mutations in any of the following genes: SDHD, SDHC, SDHB, PGL2 or other unknown genes, can cause paragangliomas (PGLs).
MATERIALS AND METHODS: We studied a Greek family in which the two daughters had carotid body paraganglioma, whereas both parents did not. RNA extraction, reverse transcriptase polymerase chain reaction and direct DNA sequencing were performed, in order to identify SDHD mutations in all four exons.
RESULTS: Our results revealed the existence of the missense mutation Y114C, in exon-4 of the SDHD gene, in the unaffected father and both affected sisters.
CONCLUSION: DNA testing was performed, for the first time in Greece, on patients with carotid body tumor. This marks a new geographical location, in the literature, for this mutation.

Entities:  

Mesh:

Substances:

Year:  2005        PMID: 16080474

Source DB:  PubMed          Journal:  Anticancer Res        ISSN: 0250-7005            Impact factor:   2.480


  2 in total

Review 1.  SDH mutations in tumorigenesis and inherited endocrine tumours: lesson from the phaeochromocytoma-paraganglioma syndromes.

Authors:  B Pasini; C A Stratakis
Journal:  J Intern Med       Date:  2009-07       Impact factor: 8.989

2.  Paraganglioma of the greater omentum: Case report and review of the literature.

Authors:  Fotios Archontovasilis; Haridimos Markogiannakis; Christina Dikoglou; Panagiotis Drimousis; Konstantinos G Toutouzas; Dimitrios Theodorou; Stilianos Katsaragakis
Journal:  World J Surg Oncol       Date:  2007-08-03       Impact factor: 2.754

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.