Journal ArticleOPEN ACCESS

Familial Paraganglioma Due to a Novel SDHB Mutation: Familial Phenotypic Heterogeneity and a Potentially Novel Manifestation

  • Alzahrani A
  • Alswailem M
  • Albattal S
  • et al.
International Journal of Endocrine Oncology (2019) 6(1)
DOI: 10.2217/ije-2018-0003
N/ACitations
Citations of this article
9Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Non-paraganglioma (PGL) tumors are rare manifestations of familial PGL syndromes. Primary hyperparathyroidism has not been described in PGL syndromes. We present a 36-year-old man with a history of...

Cite

CITATION STYLE

APA

Alzahrani, A. S., Alswailem, M., Albattal, S., Qasem, E., Murugan, A. K., & Al-Hindi, H. (2019). Familial Paraganglioma Due to a Novel SDHB Mutation: Familial Phenotypic Heterogeneity and a Potentially Novel Manifestation. International Journal of Endocrine Oncology, 6(1). https://doi.org/10.2217/ije-2018-0003

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free