Literature DB >> 24509376

SDHB gene mutation in a carotid body paraganglioma: case report and review of the paraganglioma syndromes.

Laura A Peterson1, Maria Litzendorf2, Matthew D Ringel2, Patrick S Vaccaro2.   

Abstract

Carotid body tumors represent the most common of head and neck tumors. They account for <0.03% of all human tumors. The underlying physiology and pathogenesis of this tumor type are not well understood. Several different genetic abnormalities have been associated with the development of carotid body paragangliomas. We present a case report with an unusual genetic mutation in the SDHB gene and a review of the paraganglioma syndromes.
Copyright © 2014 Elsevier Inc. All rights reserved.

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Year:  2014        PMID: 24509376     DOI: 10.1016/j.avsg.2013.12.012

Source DB:  PubMed          Journal:  Ann Vasc Surg        ISSN: 0890-5096            Impact factor:   1.466


  3 in total

1.  Familial paraganglioma syndrome: a rare cause of carotid artery occlusion.

Authors:  Francesca Rosafio; Maria Luisa Dell'Acqua; Bruno Madeo; Elda Kara; Laura Vandelli; Stefano Vallone; Guido Bigliardi; Livio Picchetto; Paolo Nichelli; Andrea Zini
Journal:  J Neurol       Date:  2016-10-20       Impact factor: 4.849

2.  Leukoencephalopathy due to Complex II Deficiency and Bi-Allelic SDHB Mutations: Further Cases and Implications for Genetic Counselling.

Authors:  Sabine Grønborg; Niklas Darin; Maria J Miranda; Bodil Damgaard; Jorge Asin Cayuela; Anders Oldfors; Gittan Kollberg; Thomas V O Hansen; Kirstine Ravn; Flemming Wibrand; Elsebet Østergaard
Journal:  JIMD Rep       Date:  2016-09-08

Review 3.  Molecular markers of paragangliomas/pheochromocytomas.

Authors:  Svetlana O Zhikrivetskaya; Anastasiya V Snezhkina; Andrew R Zaretsky; Boris Y Alekseev; Anatoly V Pokrovsky; Alexander L Golovyuk; Nataliya V Melnikova; Oleg A Stepanov; Dmitry V Kalinin; Alexey A Moskalev; George S Krasnov; Alexey A Dmitriev; Anna V Kudryavtseva
Journal:  Oncotarget       Date:  2017-04-11
  3 in total

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