Please join clinical and genetic experts from Children’s Hospital of Philadelphia for a special educational and networking event for individuals with Skraban-Deardorff syndrome and their families. This free event is open to families of any child or adult who has been diagnosed with this rare genetic disorder, or who has had a concerning change in the WDR26 gene identified through genetic testing.

Skraban-Deardorff syndrome was discovered by two physician-researchers at CHOP in 2017, who channeled their research into a clinical program to help diagnose and treat patients with the disorder. CHOP’s Skraban-Deardorff Syndrome Clinic provides comprehensive clinical services, diagnostic testing and state-of-the-art multidisciplinary care to infants, children and adolescents living with this rare disease.

Event details

Thursday to Saturday, July 28-30
8 a.m. – 5 p.m.

• Mini patient evaluations and family consultations available by appointment with Cara M. Skraban, MD, Matthew A. Deardorff, MD, PhD, Christopher Gray, MS, LCGC, and Katie Grand, MS, LCGC. (Please bring any relevant patient records or provide a Records Release to WDR26@chop.edu.)
• Scientific and clinical updates from genetic clinicians and researchers
• Professional networking and family-friendly activities

Location:
Buerger Center for Advanced Pediatric Care
Rooms 1212-1214
On the Raymond G. Perelman Campus at Children's Hospital of Philadelphia
3500 Civic Center Blvd., Philadelphia, PA 19104

Contact:
Katie Grand
grandk@chop.edu
310-423-9935