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:
Skull - short from back to front, wide on the sides, and overly tall (craniosynostosis)
Eyes - slightly side-spaced, bulging, the eyelids tilt downward abnormally at the sides
Face - the mid-face has a sunken-in appearance, the upper jaw slopes backward, lower teeth project in front of the upper teeth
Hands and feet - webbing and/or fusion including finger bones, toe bones, and joints of fingers and toes
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 many of these teams. This is by no means a comprehensive list of all the craniofacial teams. Please contact FACES for details at 800-332-2373.
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, especially Facebook groups. 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.
Apert International, Inc.
Don & Cathie Sears
P O Box 2571
Columbia, SC 29202
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.
Apert OWL is committed to providing can help families, friends and medical professionals seeking information about Apert syndrome. More importantly, we want others to know that while a journey with Apert syndrome will most definitely be a challenging one, it can be a beautiful one as well.
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.
Written by Steve Doherty
Written by the father of a child born with Apert Syndrome, Maggie 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.
National Health Law Program
1444 I Street NW, Suite 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.
Worldwide Apert Syndrome Map
A map showing where people with Apert Syndrome live. If you would like to add yourself, please do!