Home

About FACES

Client Stories

Contact Us

Craniofacial
Anomalies

Medical Centers

Paying the Bills

Adopt A Face

Newsletter Archive

FACES Events

Resources

The Independent Charities Seal of Excellence

Sign Up For Our Newletter

* First Name
* Last Name
* Email
* = Required Field
Email Marketing
You Can Trust


Make a Gift to FACES todayHow Can I Help?

Volunteer

Shop Amazon Smile

TURN TRASH INTO CASH FOR FACES

FACES UnMasked

FACES
Ride 4 Smiles

FACES Rally

Find us on Facebook Tweet us on TwitterFind us on YouTube Find us on Google+Google+

FACES: The National Craniofacial Association
(423) 266-1632
(800) 332-2373
P.O. Box 11082, Chattanooga, TN 37401





Apert Syndrome

Download PDF information sheet

Back to Craniofacial Anomalies

What is Apert Syndrome?
Apert Syndrome is a condition involving distortions of the head and face and webbing of the hands and feet. Characteristics include:

Why did this happen?
There is no link between anything the mother did or did not do while she was pregnant and the occurrence of Apert Syndrome. Doctors believe Apert Syndrome occurs when a gene mutates early in the pregnancy.

Will this happen to children I have in the future?
The chances of having another child with Apert Syndrome is almost non-existent if both parents are unaffected. If one parent has Apert Syndrome, there is a 50% chance that his/her children will have Apert Syndrome.

What kinds of problems could my child have?
In addition to the physical characteristics common to Apert Syndrome, your child may have the following problems:

Back to top

Will my child need surgery?
Depending on the severity of Apert Syndrome, your child may have some or all of the following surgeries:

New advances and procedures concerning Apert Syndrome are constantly being developed. 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
(800) 332-2373
Email: faces@faces-cranio.org
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.

Back to top

Apert International, Inc.
Don & Cathie Sears
P O Box 2571
Columbia, SC 29202
(803) 732-2372
Website: www.apert.org
This web site on Apert Syndrome will give you directions to the on-line discussion network that is an excellent support resource!!. The Annual Apert Conference is usually held each year in Myrtle Beach, South Carolina at the Crown Reef Resort. It is open to families who have been affected by Apert Syndrome or any other similar craniofacial difference. Registration is free, but families pay for travel costs, lodging, and food.

Babyface

Babyface: A Story of Heart and Bones, written by Jeanne McDermott, the mom of a son born with Apert Syndrome. This wonderful, passionate book highlights the first two years of Nate's life, and this gifted writer expresses the thoughts and feelings that are a part of the journey of having a child who is born with a rare disorder. This is a book you will want to share with your friends and family members. The book can be found at Amazon.com.

National Health Law Program
1444 I Street NW, Suite 1105
Washington, DC 20005
(202) 289-7661
Website: www.healthlaw.org
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.

The Craniofacial Center
Dr. Jeffery A. Fearon, MD, FACS, FAAP, Director
7777 Forest Lane, Suite C-700
Dallas, TX 75230
(972) 566-6464
Website: www.thecraniofacialcenter.org
Email: cranio700@gmail.com
Visit Dr. Jeffrey Fearon's informative website that is very lay friendly and easy to understand.

Back to top

-