Craniosynostosis (kray-nee-o-sin-os-TOE-sis) is a birth defect in which one or more of the fibrous joints between the bones of your baby's skull (cranial sutures) close prematurely (fuse), before your baby's brain is fully formed. Brain growth continues, giving the head a misshapen appearance.
Normally, during infancy the sutures remain flexible, giving your baby's brain time to grow. In the front of the skull, the sutures meet in the large soft spot (fontanel) on top of the head. The anterior fontanel is the soft spot you feel just behind your baby's forehead. The next largest is at the back (posterior). Each side of the skull has a tiny fontanel.
Craniosynostosis usually involves premature fusion of a single cranial suture, but can involve more than one of the sutures in your baby's skull (multiple suture craniosynostosis). In rare cases, craniosynostosis is caused by certain genetic syndromes (syndromic craniosynostosis).
Treating craniosynostosis involves surgery to correct the shape of the head and allow for normal brain growth. Early diagnosis and treatment allow your baby's brain adequate space to grow and develop.
Although neurological damage can occur in severe cases, most children have normal cognitive development and achieve good cosmetic results after surgery. Early diagnosis and treatment are key.
Craniosynostosis Care at Mayo Clinic
The signs of craniosynostosis are usually noticeable at birth, but they'll become more apparent during the first few months of your baby's life. Signs and severity depend on how many sutures are fused and when in brain development the fusion occurs. These can include:
- A misshapen skull, with the shape depending on which of the sutures are affected
- An abnormal feeling or disappearing fontanel on your baby's skull
- Development of a raised, hard ridge along affected sutures
- Slow or no growth of the head as your baby grows
Types of craniosynostosis
There are several types of craniosynostosis. Most involve the fusion of a single cranial suture. Some complex forms of craniosynostosis involve the fusion of multiple sutures. Most cases of multiple suture craniosynostosis are linked to genetic syndromes and are called syndromic craniosynostosis.
The term given to each type of craniosynostosis depends on what sutures are affected. Types of craniosynostosis include:
- Sagittal (scaphocephaly). Premature fusion of the sagittal suture that runs from the front to the back at the top of the skull forces the head to grow long and narrow. Sagittal craniosynostosis results in a head shape called scaphocephaly and is the most common type of craniosynostosis.
- Coronal. Premature fusion of one of the coronal sutures (unicoronal) that run from each ear to the top of the skull may cause the forehead to flatten on the affected side and bulge on the unaffected side. It also leads to turning of the nose and a raised eye socket on the affected side. When both coronal sutures fuse prematurely (bicoronal), the head has a short and wide appearance, often with the forehead tilted forward.
- Metopic. The metopic suture runs from the top of the bridge of the nose up through the midline of the forehead to the anterior fontanel and the sagittal suture. Premature fusion gives the forehead a triangular appearance and widens the back part of the head. This is also called trigonocephaly.
- Lambdoid. Lambdoid synostosis is a rare type of craniosynostosis that involves the lambdoid suture, which runs along the back of the head. It may cause one side of your baby's head to appear flat, one ear to be higher than the other ear and tilting of the top of the head to one side.
Other reasons for a misshapen head
A misshapen head doesn't always indicate craniosynostosis. For example, if the back of your baby's head appears flattened, it could be the result of spending too much time on one side of his or her head. This can be treated with regular position changes, or if significant, with helmet therapy (cranial orthosis) to help reshape the head to a more normal appearance.
When to see a doctor
Your doctor will routinely monitor your child's head growth at well-child visits. Talk to your pediatrician if you have concerns about your baby's head growth or shape.
Often the cause of craniosynostosis is not known, but sometimes it's related to genetic disorders.
- Nonsyndromic craniosynostosis is the most common type of craniosynostosis, and its cause is unknown, although it's thought to be a combination of genes and environmental factors.
- Syndromic craniosynostosis is caused by certain genetic syndromes, such as Apert syndrome, Pfeiffer syndrome or Crouzon syndrome, which can affect your baby's skull development. These syndromes usually also include other physical features and health problems.
If untreated, craniosynostosis may cause, for example:
- Permanent head and facial deformity
- Poor self-esteem and social isolation
The risk of increased pressure inside the skull (intracranial pressure) from simple craniosynostosis is small, as long as the suture and head shape are fixed surgically. But babies with an underlying syndrome may develop increased intracranial pressure if their skulls don't expand enough to make room for their growing brains.
If untreated, increased intracranial pressure can cause:
- Developmental delays
- Cognitive impairment
- No energy or interest (lethargy)
- Eye movement disorders
- Death, in rare instances