Session # Abstract Poster# 185

Join the paraGANGlioma - More support for FH in hereditary PGL-PCC

  • Our results support a rare subtype of HLRCC in which PCC is the predominant finding.
  • Interlaboratory collaboration aids in accurate variant classification.
  • A better understanding of the prevalence of this disease subtype and penetrance of PCC in affected families is needed in order to identify other at risk individuals and guide management.

  • Authors: Carrie Horton; Marcy Richardson; Min-Sun Park; Michael Anderson; Huma Rana
  • Collaborators: Dana Farber Cancer Institute
  • Conference: Annual Clinical Genetics Meeting (ACMG) 2019
  • Date: Thursday, Apr 04, 2019 10:00am - 11:30am

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