Binder Syndrome

Also known as: Binder type, nasomaxillary hypolasia, maxillafacial dysplasia.

What is Binder syndrome?

Binder syndrome is a congenital disorder characterized by a flat, underdeveloped midface and nose. The jaw might also be affected, and the face may appear imbalanced.

What causes Binder syndrome?

The exact cause of Binder syndrome is unclear. It may be a genetic disorder, and it appears to run in families in some cases.

What are the symptoms of Binder syndrome?

The flattened midface is the primary symptom of Binder syndrome. This may result in a recessed upper jaw and misaligned teeth (malocclusion). When the nose is affected, it is characterized by a flat nasal bridge and a short columella.

What are Binder syndrome care options?

Treatment for Binder syndrome will vary depending on what specific abnormalities are present. Reconstructive surgery may be an option to help with issues related to the face. Typically, correction of the recessed upper jaw is performed when the facial bones have finished growing, around 16-18 years of age, with a procedure known as LeFort I advancement. This is usually preceded and followed by orthodontic treatment.

The nasal deformity can be corrected around the same time with a septorhinoplasty and placement of a bone graft.

Reviewed by: Saoussen Salhi, MD

This page was last updated on: 7/12/2018 1:57:21 PM

From the Newsdesk

Bianca’s Journey to Being Pain Free
Bianca suffered from pain and a severe bowleg deformity for many years as a result of Blount’s disease, a growth disorder that affects the bones in children and young adults.
South Florida hospital is leader in treating apert syndrome
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.