This conference was made possible thanks to generous support from
The University of Florida
The Int'l 22q11.2 Deletion Syndrome Foundation
and The Florida VCFS Support Group

OVERVIEW
The 22q11.2 deletion syndrome is a recognizable pattern of physical and developmental features associated with a missing section (deletion) of genetic material on chromosome 22. The condition is sometimes referred to as velo-cardio-facial syndrome, Shprintzen syndrome, or DiGeorge syndrome. The effects of the deletion include a variety of physical findings, such as heart abnormalities, cleft palate, immune deficiencies, and a characteristic facial appearance. In addition, children with the 22q11.2 deletion syndrome show a spectrum of developmental issues, including learning, social, and emotional disabilities. This conference will focus on the educational and behavioral features associated with the syndrome, as well as practical strategies for addressing these needs. To learn more about the 22q11.2 deletion syndrome, visit:

• The International 22q11.2 Deletion Syndrome Foundation
• Chromosome 22 Central
• The Velo-Cardio-Facial Syndrome Educational Foundation

AGENDA AND FACULTY
Click here to see the schedule, topics, and speakers

WHAT WILL I GAIN FROM ATTENDING THIS CONFERENCE?  
As a result of this conference, participants will be able to:

      - recognize the spectrum of physical, behavioral, and cognitive features seen in children

        with deletions of chromosome 22q11.2

      - distinguish behavioral diagnoses, like ADHD and autism, from causal diagnoses, such

        as 22q11.2 deletion syndrome

      - apply educational and behavioral strategies for working with students who have

           22q11.2 deletion syndrome

      - access informational and therapeutic resources on 22q11.2 deletion syndrome

WHO SHOULD ATTEND?   

This conference will be of interest to parents, special educators, psychologists, genetics professionals, nurses, social workers, parents, and others involved in the care of school-aged children and adolescents with the 22q11.2 deletion syndrome. The focus will be on practical and understandable information.

WHAT IS THE COST?

The conference fee includes all sessions, materials, as well as continental breakfast and lunch on Saturday and Sunday. Discounted registration is offered for groups of 3 or more people registering together. Family members and individuals with the deletion are also offered a discounted rate. Registration is free for children under 14. Fees are as follows:

           - $100  per person for 1 or 2 professionals

           - $ 90  per person for 3 or more professionals registering together

           - $ 90  per family member / individual with the 22q11.2 deletion

HOW DO I REGISTER? 
Click here to register

WHO CAN I CONTACT FOR MORE INFORMATION?

Brenda Finucane, MS, CGC

Executive Director, Genetic Services at Elwyn

Phone: 610-891-2313,  Fax: 610-891-2377

brenda_finucane@elwyn.org