|P. O. Box 11082||* Chattanooga, TN 37401|
Pierre Robin Sequence
What is Pierre Robin?
Pierre Robin is not a syndrome or a disease. It is usually referred to as Pierre Robin Sequence, although it is also know as "Pierre Robin Malformation Sequence", "Robin Anomalad", and "Cleft Palate, Micrognathia and Glossoptosis." It is the name given to the following birth defects if they appear together:
Why did this happen?
Doctors do no know exactly why Pierre Robin occurs. They do not believe it is the result of anything the mother did or did not do during pregnancy. If the child only has Pierre Robin, many experts believe that it is the result of the positioning of the fetus in the early weeks of pregnancy.
Will this happen to children I have in the future?
Pierre Robin does not tend to run in families. The chances of you having another child with Pierre Robin are very small, unless the Pierre Robin Sequence is a part of a syndrome.
What kinds of problems could my child have?
In addition to the physical characteristics common to Pierre Robin, your child may have the following problems:
Will my child need surgery?
Depending on the severity of Pierre Robin, your child may have some or all of the following surgeries:
New advances in procedures to correct the problems associated with Pierre Robin are constantly being made. Be an advocate for your child!
How do I get help for my child?
Your child should be treated by a qualified craniofacial medical team at a craniofacial center. Currently, FACES has information on sixty-four craniofacial teams located in 27 states, the District of Columbia, and Canada. This is by no means a comprehensive list of all the craniofacial teams. Please contact FACES for details.
Am I alone?
No! There are many families and organizations who will be glad to talk with you and help you with information and support. Don't forget books, videos, and websites. The listing below will get you started.
FACES: The National Craniofacial Association
P. O. Box 11082
Chattanooga, TN 37401
We provide financial support for non-medical expenses to patients traveling to a craniofacial center for treatment. Eligibility is based on financial and medical need. Resources include newsletters, information about craniofacial conditions, and networking opportunities.
Pierre Robin Network
P. O. Box 3274
Quincy, IL 62305
This is an internet support group composed of parents who are networking together to offer support to each other. There is also an outreach committee available to talk to those without internet access.
The Cleft Palate Foundation (CPF)
1504 E. Franklin St., Ste. 102
Chapel Hill, NC 27514
Resources include 24-hour information phone, fact sheets on cleft lip and palate and Pierre Robin, brochures, and medical referrals.
The Cleft Palate Story. Written by Samuel Berkowitz, DDS, MS,
FICD. Published by Quintessence Publishing Co., 1-800-621-0387.
Surgical procedures performed from birth to adolescence are treated in depth; helps parents to understand options and what to expect; appendices on financial assistance, agencies, support groups, and a glossary of terms.
National Health Law Program
1444 I St., NW, Ste. 1105
Washington, DC 20005
Provides extensive information on health care law affecting families with children who have special health care needs.
Children with Facial Difference: A Parent's Guide.
Written by Hope Charkins, MSW. Order from Amazon.com if you cannot find it in your local bookstore.
Excellent resource for parents to help them cope with medical, emotional, social, educational, legal, and financial challenges presented by facial differences of their children.
National Parent to Parent Organization
c/o Julie Gordon
150 Custer Court
Green Bay, WI 54301-1243
Toll free (877) 336-5333
This organization helps you get in touch with parents
in your area whose children also have Pierre Robin.
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Last modified on: Thursday, February 10, 2011 02:56 PM