Elizabeth Petty, MD

Neonatal Progeroid Syndrome: Lipodystrophy; Craniofacial, Dental, Ocular & Digital Anomalies; and Short Stature

  • Summarize the key clinical and molecular features of the neonatal onset progeroid syndrome discussed.
  • Illustrate the utility of collaboration, updated literature reviews, long-term patient follow-up, and repeat genetic/genomic testing for individuals with multiple systemic features with unknown conditions/syndromes. 
  • Evaluate the pros and cons of using eponyms for genetic syndromes.

 

Luke Stavedahl, BS

Ashley Kuhl, MS, CGC

Incidental Findings in Panel Testing for Sensorineural Hearing Loss

  • Identify different causes of sensorineural hearing loss.
  • Summarize the pathophysiology of the genetic cause of deafness-infertility syndrome​.
  • Examine techniques for discussing infertility and other difficult topics with patients.

 

Session date: 
01/15/2025 - 4:00pm to 5:00pm CST
Location: 
Virtually
WI 53705
United States
See map: Google Maps
  • 1.00 AAPA Category 1 CME
  • 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): 
Luke Stavedahl, BS (grad student)
Ashley Kuhl, MS, CGC
Elizabeth Petty, MD