Also known as: Premature closure of sutures, Synostosis, Plagiocephaly, Scaphocephaly, Fontanelle - craniosynostosis or Soft spot - craniosynostosis
- No "soft spot" (fontanelle) on the newborn's skull
- A raised hard ridge along the affected sutures
- Unusual head shape
- Slow or no increase in the head size over time as the baby grows
- Sagittal synostosis (scaphocephaly) is the most common type. It affects the main suture on the very top of the head. The early closing forces the head to grow long and narrow, instead of wide. Babies with this type tend to have a broad forehead. It is more common in boys than girls.
- Frontal plagiocephaly is the next most common type. It affects the suture that runs from ear to ear on the top of the head. It is more common in girls.
- Metopic synostosis is a rare form that affects the suture close to the forehead. The child's head shape may be described as trigonocephaly. It may range from mild to severe.
- Relieve any pressure on the brain
- Make sure there is enough room in the skull to allow the brain to properly grow
- Improve the appearance of the child's head
- How many sutures are involved
- The child's overall health
- You think your child's head shape is unusual.
- Your child is not growing well.
- The child has unusual raised ridges on the scalp.
Craniosynostosis is a birth defect in which one or more of the sutures on a baby's head closes earlier than usual.
The skull of an infant or young child is made up of bony plates that allow for growth of the skull. The borders at which these plates intersect are called sutures or suture lines. The sutures between these bony plates normally close by the time the child is 2 or 3 years old.
Early closing of a suture causes the baby to have an abnormally shaped head and may limit brain growth.
The cause of craniosynostosis is unknown. Genes may play a role, but there is usually no family history of the condition.
One type that is passed down through families (inherited) can occur with other health problems, such as seizures, decreased intelligence, and blindness. Genetic disorders commonly linked to craniosynostosis include Crouzon, Apert, Carpenter, Saethre-Chotzen, and Pfeiffer syndromes.
However, most children with craniosynostosis are otherwise healthy and have normal intelligence.
Symptoms depend on the type of craniosynostosis. They may include:
Types of craniosynostosis:
Exams and Tests
The health care provider will feel the infant's head and perform a physical exam.
The following tests may be done:
Well-child visits are an important part of your child's health care. They allow your provider to regularly check the growth of your infant's head over time. This will help identify any problems early.
Surgery is done while the baby is still an infant. The goals of surgery are:
How well a child does depends on:
Children with this condition who have surgery do well in most cases, especially when the condition is not associated with a genetic syndrome.
Craniosynostosis results in head deformity that can be severe and permanent if it is not corrected. Increased intracranial pressure, seizures, and developmental delay can occur.
When to Contact a Medical Professional
Call your child's provider if:
Graham JM, Sanchwez-Lara PA. Craniosynostosis. In: Graham JM, Sanchez-Lara PA, eds. Smith's'Recognizable Patterns of Human Deformation. 4th ed. Philadelphia, PA: Elsevier; 2016:chap 29.
Kinsman SL, Johnston MV. Craniosynostosis. In: Kliegman RM, Stanton BF, St Geme JW, Schor NF, eds. Nelson Textbook of Pediatrics. 20th ed. Philadelphia, PA: Elsevier; 2016:chap 591.
- Review date:
- March 11, 2015
- Reviewed by:
- Kimberly G. Lee, MD, MSc, IBCLC, Associate Professor of Pediatrics, Division of Neonatology, Medical University of South Carolina, Charleston, SC. Review provided by VeriMed Healthcare Network. Also reviewed by David Zieve, MD, MHA, Isla Ogilvie, PhD, and the A.D.A.M. Editorial team.
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