fbpx Skip to main content

Conditions & Diseases

Craniosynostosis

What is Craniosynostosis?

Craniosynostosis, also known as craniostenosis or simply synostosis, is a congenital condition characterized by the premature fusion of one or more sutures (joints) between the bones of a baby’s skull. Normally, a baby’s skull is composed of several bones separated by sutures, allowing the skull to expand as the brain grows. However, in craniosynostosis, these sutures close too early, hindering proper skull development and potentially leading to various health issues.

Has your child been diagnosed with Craniosynostosis?

Get started with Healwise to receive free and professional healthcare assistance from start to finish.
Submit your information today and get treatment & hospital recommendations fast, with no obligation to commit.

Get Started

Symptoms

The symptoms of craniosynostosis can vary depending on which sutures close prematurely and to what extent. Common signs and symptoms may include:

  • Abnormal head shape: One of the most noticeable signs is an irregular head shape, which can manifest as a flattened or pointed skull.

  • Delayed fontanelle closure: The fontanelles (soft spots) on a baby’s head typically close by a certain age. In craniosynostosis, the affected fontanelles may close earlier or later than expected.

  • High or prominent forehead: Some forms of craniosynostosis result in an unusually shaped forehead.

  • Raised ridges along sutures: In areas where the sutures have prematurely fused, raised ridges or hard lumps may be felt on the baby’s skull.

  • Increased intracranial pressure: In severe cases, craniosynostosis can lead to increased pressure within the skull, potentially causing developmental delays, vision problems, or other neurological issues.

  • Sleep apnea: Craniosynostosis may lead to sleep apnea, characterized by pauses in breathing during sleep, which can affect the baby’s quality of sleep.

  • Feeding difficulties: Some babies with craniosynostosis may have difficulty feeding due to their skull shape.

Diagnosis

Diagnosing craniosynostosis typically involves a combination of physical examinations, imaging studies, and medical history assessments. A healthcare provider will examine the baby’s head shape, fontanelles, and sutures. Imaging studies like X-rays, CT scans, or MRIs may be used to visualize the skull’s structure and confirm the diagnosis. Additionally, genetic testing may be recommended to check for any underlying genetic factors associated with craniosynostosis.

Treatment

The treatment of craniosynostosis primarily depends on the severity of the condition and the specific sutures involved. Treatment options include:

  • Observation: In mild cases where the condition does not significantly affect the baby’s head shape or health, regular monitoring may be recommended.

  • Surgery: Surgical intervention is often necessary to correct craniosynostosis. The main goal of surgery is to release the prematurely fused suture and reshape the skull to allow for proper brain growth. The timing of surgery is crucial and depends on the baby’s age and the type of craniosynostosis.

    • Open Cranial Vault Remodeling: This is the most common surgical procedure, involving an open approach to release the fused suture, followed by reshaping the skull. It is typically performed during the first year of life.

    • Endoscopic Surgery: In some cases, minimally invasive endoscopic surgery may be an option. Small incisions are made to access the suture, allowing for its release and subsequent reshaping of the skull.

  • Helmet Therapy: In mild cases or as a postoperative measure, helmet therapy may be recommended. Helmets are custom-made to help mold the baby’s head into a more normal shape as they grow.

  • Physical Therapy: Some babies with craniosynostosis may require physical therapy to address issues related to head positioning and movement.

  • Monitoring: Regular follow-up visits with healthcare providers are essential to track the baby’s progress and ensure that the skull is growing appropriately.

Early diagnosis and intervention are crucial for the successful treatment of craniosynostosis. Prompt medical attention and individualized treatment plans can lead to improved head shape, normal brain development, and an overall better quality of life for affected children.

Craniosynostosis is a condition where one or more sutures (joints) between the bones of a baby’s skull close prematurely. This can lead to an irregular head shape and, in severe cases, increased intracranial pressure and developmental issues. Diagnosis involves physical exams and imaging studies, while treatment options range from observation to surgery, depending on the severity. Timely intervention is essential for optimal outcomes.

Healwise provides solutions for individuals facing health challenges like Craniosynostosis. Our platform offers access to specialized interventions such as Open Cranial Vault Remodeling and Endoscopic Surgery. Open Cranial Vault Remodeling is a surgical procedure that addresses the fusion of cranial sutures in infants, allowing for proper skull development. Additionally, Endoscopic Surgery provides a minimally invasive alternative, minimizing scarring and reducing recovery time.

See All Treatments & Prices

Find Free & Quick Help with Healwise

Discover top doctors who can treat Craniosynostosis.

Healwise gives you top neurosurgery expert recommendations in nearby countries, and supports you from start to finish. All at no extra cost to you.

Get Started