Mission Statement

Welcome to the Chromosome 3 Disorder Registry and Support Group. The mission of our group is to provide information and emotional support to families, friends and professionals who would like to learn more about children/family members affected by a Chromosome 3 disorder.  When many of us first learned of our child’s or family member’s rare chromosomal disorder, we had to search far and wide to get answers, common symptoms, possible matches to our family member, and information about chromosomes.  Many of us have researched or experienced ways to help our children thrive and are hoping to share some of these ideas with you.

While no two children are exactly alike (even with the same deletion), we do notice there are many similarities and overlapping symptoms in many of the children. We know how devastating it can be initially to find out your child has a chromosomal disorder or any genetic defect for that matter. We are hoping that if you are a new parent/relative to a child with a chromosome 3 disorder, you will be better equipped with information and will have the ability to more easily prepare for a future with your child/family member.

Rules and Guidelines

By participating on this website you understand and agree to comply with the following rules and regulations:

Not to post any information which may be construed in any way to be a solicitation benefiting any individual or entity other than Chromosome3disorder.com.

Chromosome3disorder.com reserves the right in their sole discretion to remove any information or content that, in their sole judgment, has any harmful, objectionable, inaccurate information or is slanderous. Chromosome3disorder.com is not responsible for the delay in removing any content.

The member stories and other content in the website do not necessarily reflect the feelings/opinions of chromosome3disorder.com.  Parents/guardians/family members agree that the information in the pages in this website are updated by each member listed in the member stories or a family member who is either a guardian or approved by the guardian to post content about the family member with the chromosome 3 disorder.

Always check with your doctor if you have any questions, concerns or to check the validity of any information provided in this website.  Chromosome3disorder.com is not responsible for any losses or damage of any kind incurred as a result of the use of or reliance on any information posted in this website. Chromosome3disorder.com does not warrant or guarantee the accuracy of any information on this website or any links to information that may be on any other website.

You expressly understand & agree that you bear all risks associated with using or relying on this information.