Megan Benoy, MS, CGC

Secondary Familial Hypercholesterolemia Findings on WES

  • Identify signs of when to suspect Familial Hypercholesterolemia (FH).
  • Examine cases where FH was identified on Whole Exome Sequencing (WES).
  • Illustrate the need for appropriate referrals and interventions in these patients.

 

Becky Pulvermacher, BS

Kalyn Stroik, MS, CGC

A Rare Find: EBF3-related Neurodevelopmental Disorder with Multiple Anomalies

  • Identify differential diagnoses for certain congenital anomalies.
  • Examine the appropriate genetic testing protocol given a complex medical history with multiple congenital anomalies.
  • Summarize clinical and molecular findings suggestive of EBF3-related neurodevelopmental disorder with multiple anomalies.
Session date: 
04/03/2024 - 4:00pm to 5:00pm CDT
Location: 
Virtual
WI
United States
See map: Google Maps
  • 1.00 AMA PRA Category 1 Credit™
  • 1.00 ANCC Contact Hours
  • 1.00 CDR CPEUs
  • 1.00 NSGC Category 1 CEU Contact Hours
  • 1.00 University of Wisconsin–Madison Continuing Education Hours
    • 1.00 Approved for AMA PRA Category 1 Credit™
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Discloser List CME Internal Report
Presenter(s): 
Megan Benoy, MS, CGC
Becky Pulvermacher, BS (grad student)
Kalyn Stroik, MS, CGC