The information contained in the Organizational Database (ODB) is provided for informational purposes only. There is no implied endorsement by NORD. NORD does not promote or endorse participation in any specific organization. The information is subject to change without notice. Every effort is made to ensure that the details for each entry are as current as possible.
The Children's Hospital of Philadelphia
3401 Civic Center Blvd
Philadelphia, PA 19104 USA
215-590-2920
800-879-2467
The "22q and You" Center, at The Children's Hospital of Philadelphia, provides state of the art diagnosis, treatment and follow-up services for individuals and families affected by chromosome 22q11.2 abnormalities, including deletions, duplications, and gene mutations within this region of chromosome 22. In addition, we continue to lead conduct research and provision of coordinated care while striving to understand etiologies and best treatment strategies. Our staff includes clinicians and scientists with expertise in all facets of basic science and clinical care. We have evaluated more than 1,000 patients with differences in chromosome 22q11.2,. While many of our patients reside within the Mid-Atlantic states, we serve the broader North American and international community as well, with families traveling to us from throughout the continental United States, Alaska, Hawaii, Canada, and abroad, including such distant locations as Australia, England, France, Germany, Ireland, Israel and Ukraine.
Please Note
The National Organization for Rare Disorders (NORD) web site, its databases, and the contents thereof are copyrighted by NORD. No part of the NORD web site, databases, or the contents may be copied in any way, including but not limited to the following: electronically downloading, storing in a retrieval system, or redistributing for any commercial purposes without the express written permission of NORD. Permission is hereby granted to print one hard copy of the information on an individual disease for your personal use, provided that such content is in no way modified, and the credit for the source (NORD) and NORD’s copyright notice are included on the printed copy. Any other electronic reproduction or other printed versions is strictly prohibited.
NORD's Rare Disease Information Database is copyrighted and may not be published without the written consent of NORD.
