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:
- cleft palate - about 30% of children with Apert Syndrome are affected
- slower learning rates and abilities - about 50% of children with Apert Syndrome are affected; however, as the children grow older, they often catch up with others
- vision problems caused by imbalance of the eye muscles
- recurrent ear infections which can cause hearing loss
- noisy breathing - the smaller nose and airway passages may make breathing difficult
- hyperactive sweat glands may cause your child to sweat a lot, especially while sleeping
- problems with acne are more likely, especially during puberty
Will my child need surgery?
Depending on the severity of Apert Syndrome, your child may have some or all of the following surgeries:
- total skull reshaping to correct the tower skull problems at three to four months of age
- frontal-orbital advancement to increase space within the skull and the size of both orbits (the part of the skull with holds the eyeball) at three to four months of age
- mid-facial advancement - usually prior to starting school
- facial bi-partition to widen the upper jaw, derotate the orbits, and to narrow the upper face
- osteotomy (cutting through the bone of the upper and lower jaw to correct further problems usually during the teen years
- rhinoplasty - plastic surgery of the nose
- genioplasty - plastic surgery of the chin or cheek
- eyelid surgery to correct the abnormal downward tilt
- separation of the fingers and/or toes
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 thirty-two craniofacial teams located in 20 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.
Apert International, Inc.
Don & Cathie Sears
P O Box 2571
Columbia, SC 29202
(803) 732-2372
Website: http://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 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. For more information, call Cathy Sears at 803-732-2372 or go to www.apert.org.
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 is published by Woodbine House and is also available at most major bookstores.
National Health Law Program
1101 14th Street, NW, Suite 405
Washington, DC 20005
(202) 289-7661
Website: http://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. Published by Woodbine House, 1996. (800) 843-7323.
Excellent resource for parents to help them cope with medical, emotional, social, educational, legal, and financial challenges presented by facial differences of their children.
AboutFace USA
P. O. Box 969
Batavia, IL 60510
Toll free (888) 486-1209
Email: aboutfaceus@aol.com
Ask for a copy of the AboutFace booklet on Apert Syndrome.
The Craniofacial Center
Dr. Jeffery A. Fearon, MD, FACS, FAAP, Director
7777 Forest Lane, Suite C-700
Dallas, TX 75230
(972) 566-6464
Email: cranio700@aol.com
Visit Dr. Jeffrey Fearon's informative website that is very lay friendly and easy to understand.
Maggie
Written by Steve Doherty
Published by Seaview Press Pty Ltd
186 Seaview Road, P O Box 234
Henley Beach, SA 5022 AUSTRALIA
Phone: 61-8-8235-1535
Email: seaview@seaviewpress.com.au
Website: http://www.seaviewpress.com.au
Written by the father of a child born with Apert Syndrome, Maggie is a delightful and insightful little book that takes the reader on the adventure of having a child born with Apert Syndrome, through all of its ups, downs, trials, and triumphs. A true love story.
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