To Top
0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z


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.

International Children’s Anophthalmia Network (ICAN)


c/o Center for Devel Medicine & Genetics
5501 Old York Road
Philadelphia, PA 19141 USA





800 Number


Email Address

[email protected]


The International Children's Anophthalmia Network (ICAN), a voluntary, non-profit organization, is a group of families and professionals dedicated to lending support to individuals who want to learn more about microphthalmia and anophthalmia (eyes that are abnormally small, completely absent, or consist only of vestigial portions). Members of this network are offered the opportunity to enroll in the Anophthalmia/Microphthalmia Registry, which was established to identify all syndromes associated with anophthalmia/ microphthalmia, describe the spectrum of associated anomalies, and investigate whether any teratogens are involved in the etiology of anophthalmia/microphthalmia. The network also enables parents with affected children to share personal experiences, information, and support; take advantage of its database of physicians and educational resources; and learn about ongoing research and medical issues. It provides referrals to genetic counseling, support groups, and other services and promotes professional and patient education, as well as a variety of educational and support materials. A program of screening for eye development gene mutations was initiated in 1999 and is ongoing with the participation of eight labs worldwide. It is coordinated through the Genetics Division at Albert Einstein Medical Center in Philadelphia and supported by the members of ICAN.

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.