Also known as: CCM syndrome, CCMS.
What is cerebrocostomandibular syndrome?
Cerebrocostomandibular syndrome is an extremely rare congenital disorder that impacts the jaw and mouth. Infants with the disease have a small jaw (micrognathia), malformations of the roof of the mouth (cleft palate), malposition of the tongue (glossoptosis) and abnormal development of the ribs (rib dysplasia).
What causes cerebrocostomandibular syndrome?
The cause of cerebrocostomandibular syndrome is not entirely clear. There may be a genetic component to the disease, and it appears to run in families in some cases.
What are the symptoms of CCMS?
The abnormal rib development can cause breathing difficulties for the infant. Defects of the roof of the mouth can cause feeding and speech difficulites. Most individuals affected by this syndrome exhibit normal intelligence. However, some can have delay in mental development.
What are CCMS care options?
Many specialists may be involved in the care of infants with cerebrocostomandibular syndrome, particularly for the immediate concerns of breathing and feeding. Though there is no cure for the disease, there are several therapies and surgical options that can help children with the disease.
Reviewed by: Saoussen Salhi, MD
This page was last updated on: 7/12/2018 2:03:57 PM
From the Newsdesk
Dr. Chad Perlyn and Dr. Mislen Bauer from the Nicklaus Children's Craniofacial Center are committed to helping families and children with apert syndrome. Check out this segment featured on WPLG Local 10.
Families from all around the world traveled to Nicklaus Children’s Hospital in July for an educational conference about Beckwith-Wiedemann Syndrome (BWS), a congenital, genetic condition that can cause premature birth, hypoglycemia, abdominal wall defects, abdominal malignancies and macroglossia (englarged tongue).