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: ACMG 2019
• Date: Thursday, Apr 04, 2019 10:00am - 11:30am