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Endoscopic Suturectomy

A Minimally Invasive Option for Craniosynostosis Treatment

For parents facing a diagnosis of craniosynostosis, the decision about which surgical approach is best for their child can feel overwhelming. Traditional open surgery, known as cranial vault remodeling (CVR), has been the standard treatment for decades. However, endoscopic suturectomy has emerged as a minimally invasive alternative that, for the right candidate, can offer excellent outcomes with a shorter surgery, less blood loss, and a faster recovery. This technique, when combined with postoperative helmet therapy, allows a baby’s skull to reshape naturally as it grows.

Understanding how endoscopic suturectomy works, who qualifies, and what the recovery process involves can help parents make an informed decision alongside their craniofacial specialist. Unlike open surgery, which involves large incisions and the immediate reconstruction of the skull, endoscopic suturectomy relies on the body’s natural growth process. By removing the fused suture through small incisions, the procedure allows the skull to expand in the proper direction over time. This method works best when performed very early in infancy, usually before three months of age, when the skull is still flexible and able to be guided by a custom helmet worn for several months after surgery.

This chapter will explain who is a good candidate for endoscopic suturectomy, what happens during surgery, and what parents should expect before, during, and after the procedure. It will also explore how helmet therapy plays a critical role in ensuring the best results, as well as how this approach compares to traditional surgery. By the end, parents will have a clear understanding of whether this minimally invasive procedure might be the right choice for their child.

Indications & Patient Selection

Endoscopic suturectomy is a highly effective treatment for craniosynostosis, but it is not the right option for every child. Unlike traditional open surgery, which can be performed later in infancy, this minimally invasive approach relies on the skull’s natural ability to reshape during early growth. The timing of the procedure and the specific type of craniosynostosis will determine whether your child is a good candidate. Understanding the selection criteria can help you decide whether this procedure is the best choice for your baby.

Ideal Candidates for Endoscopic Suturectomy

  • Unilateral Coronal
  • Lambdoid
Sagittal

Metopic

Overview

Metopic synostosis, also known as trigonocephaly, is characterized by the premature fusion of the metopic suture, which runs from the top of the head down the middle of the forehead to the nose. This fusion results in a triangular-shaped forehead and a prominent ridge along the suture line.

metopic

Incidence

The overall incidence of Craniosynostosis is approximately 1 in 2000/3000 births. Metopic synostosis is relatively rare, accounting for between 5% and 15% of all craniosynostosis cases.

Diagnosis

Diagnostically, the condition can be identified through a physical examination, where the triangular shape of the forehead and ridging are noticeable. Imaging techniques, such as computed tomography (CT) scans, can confirm the diagnosis and assess the extent of the fusion.

Treatment

Treatment typically involves surgery to correct the skull shape and allow for normal brain growth. The surgical procedure, usually performed in the first year of life, involves removing and reshaping the fused bones to create a more typical skull contour. Please refer to our Treatment Options page for a more detailed explanation of these surgical procedures.

Overview

This is the most common type of single-suture craniosynostosis, where the sagittal suture (running from front to back along the top of the head) fuses prematurely, causing an elongated skull. Endoscopic release allows the head to widen over time with helmet therapy.

metopic
Incidence

The overall incidence of Craniosynostosis is approximately 1 in 2000/3000 births. Metopic synostosis is relatively rare, accounting for between 5% and 15% of all craniosynostosis cases.

Diagnosis

Diagnostically, the condition can be identified through a physical examination, where the triangular shape of the forehead and ridging are noticeable. Imaging techniques, such as computed tomography (CT) scans, can confirm the diagnosis and assess the extent of the fusion.

Treatment

Treatment typically involves surgery to correct the skull shape and allow for normal brain growth. The surgical procedure, usually performed in the first year of life, involves removing and reshaping the fused bones to create a more typical skull contour. Please refer to our Treatment Options page for a more detailed explanation of these surgical procedures.

Metopic

Coronal

Overview

Premature closure of the metopic suture (running from the forehead to the top of the skull) results in a triangular-shaped forehead. In mild to moderate cases, endoscopic suturectomy may allow for gradual correction. However, more severe cases may still require open surgery.

posterior cranioynostosis
Incidence

The overall incidence of Craniosynostosis is approximately 1 in 2000/3000 births. Coronal synostosis accounts for approximately 20% to 30% of all craniosynostosis cases.

Diagnosis

Diagnosis of coronal synostosis involves a thorough physical examination where asymmetry or brachycephaly is apparent. Imaging techniques, including CT scans, help confirm the diagnosis and plan the surgical intervention.

Treatment

Surgical correction is typically recommended to improve skull shape and symmetry. The timing of the surgery is crucial; it is often performed within the first year of life to maximize the benefits. Procedures may involve fronto-orbital advancement and reshaping of the forehead and eye sockets. Please refer to our Treatment Options page for a more detailed explanation of these surgical procedures.

Overview

Coronal synostosis involves the premature fusion of one (unilateral) or both (bilateral) coronal sutures, which run from ear to ear over the top of the skull. Unilateral coronal synostosis, also known as synostotic anterior plagiocephaly, results in an asymmetrical skull with a flattened forehead on the affected side and a raised eyebrow. Bilateral coronal synostosis, also known as brachycephaly, leads to a brachycephalic head shape, characterized by a broad, short skull.

Synostotic Anterior Plagiocephaly

Incidence

The overall incidence of Craniosynostosis is approximately 1 in 2000/3000 births. Coronal synostosis accounts for approximately 20% to 30% of all craniosynostosis cases.

Diagnosis

Diagnosis of coronal synostosis involves a thorough physical examination where asymmetry or brachycephaly is apparent. Imaging techniques, including CT scans, help confirm the diagnosis and plan the surgical intervention.

Treatment

Surgical correction is typically recommended to improve skull shape and symmetry. The timing of the surgery is crucial; it is often performed within the first year of life to maximize the benefits. Procedures may involve fronto-orbital advancement and reshaping of the forehead and eye sockets. Please refer to our Treatment Options page for a more detailed explanation of these surgical procedures.

Unilateral Coronal

Sagittal

Overview

Fusion of one coronal suture (running from the ear to the top of the head) leads to forehead flattening and orbital asymmetry. Endoscopic release can be effective if diagnosed early, but helmet therapy is crucial for guiding correction.

Scaphocephaly
Incidence

The overall incidence of Craniosynostosis is approximately 1 in 2000/3000 births. Sagittal synostosis accounts for approximately 40% to 55% of all craniosynostosis cases.

Diagnosis

Physical examination often reveals a long, narrow head shape with a prominent ridge along the sagittal suture. Confirmatory diagnosis is achieved through imaging studies such as CT scans, which provide detailed views of the fused suture and skull shape.

Treatment

Surgical treatment for sagittal synostosis aims to expand the width of the skull and improve its overall shape. Depending on the severity of the condition, procedures may include minimally invasive endoscopic suturectomy or a more complex procedure referred to as cranial vault remodeling. Please refer to our Treatment Options page for a more detailed explanation of these surgical procedures.

Overview

Sagittal synostosis, also known as scaphocephaly, is the most common form of craniosynostosis. It involves the premature fusion of the sagittal suture, which runs from the front to the back of the skull along the midline. This fusion causes the head to grow long and narrow, a condition known as scaphocephaly.

Synostotic Anterior Plagiocephaly

Incidence

The overall incidence of Craniosynostosis is approximately 1 in 2000/3000 births. Sagittal synostosis accounts for approximately 40% to 55% of all craniosynostosis cases.

Diagnosis

Physical examination often reveals a long, narrow head shape with a prominent ridge along the sagittal suture. Confirmatory diagnosis is achieved through imaging studies such as CT scans, which provide detailed views of the fused suture and skull shape.

Treatment

Surgical treatment for sagittal synostosis aims to expand the width of the skull and improve its overall shape. Depending on the severity of the condition, procedures may include minimally invasive endoscopic suturectomy or a more complex procedure referred to as cranial vault remodeling. Please refer to our Treatment Options page for a more detailed explanation of these surgical procedures.

Lambdoid

Sagittal

Overview

Fusion of the lambdoid suture (at the back of the skull) causes a flattened appearance on one side. This type is less common, but when caught early, endoscopic treatment may provide good results.

Scaphocephaly
Incidence

The overall incidence of Craniosynostosis is approximately 1 in 2000/3000 births. Sagittal synostosis accounts for approximately 40% to 55% of all craniosynostosis cases.

Diagnosis

Physical examination often reveals a long, narrow head shape with a prominent ridge along the sagittal suture. Confirmatory diagnosis is achieved through imaging studies such as CT scans, which provide detailed views of the fused suture and skull shape.

Treatment

Surgical treatment for sagittal synostosis aims to expand the width of the skull and improve its overall shape. Depending on the severity of the condition, procedures may include minimally invasive endoscopic suturectomy or a more complex procedure referred to as cranial vault remodeling. Please refer to our Treatment Options page for a more detailed explanation of these surgical procedures.

Overview

Sagittal synostosis, also known as scaphocephaly, is the most common form of craniosynostosis. It involves the premature fusion of the sagittal suture, which runs from the front to the back of the skull along the midline. This fusion causes the head to grow long and narrow, a condition known as scaphocephaly.

Synostotic Anterior Plagiocephaly

Incidence

The overall incidence of Craniosynostosis is approximately 1 in 2000/3000 births. Sagittal synostosis accounts for approximately 40% to 55% of all craniosynostosis cases.

Diagnosis

Physical examination often reveals a long, narrow head shape with a prominent ridge along the sagittal suture. Confirmatory diagnosis is achieved through imaging studies such as CT scans, which provide detailed views of the fused suture and skull shape.

Treatment

Surgical treatment for sagittal synostosis aims to expand the width of the skull and improve its overall shape. Depending on the severity of the condition, procedures may include minimally invasive endoscopic suturectomy or a more complex procedure referred to as cranial vault remodeling. Please refer to our Treatment Options page for a more detailed explanation of these surgical procedures.

Syndromic

Lambdoid

Overview

For babies with multiple fused sutures or syndromic craniosynostosis (such as Apert, Crouzon, or Pfeiffer syndromes), endoscopic suturectomy is typically not the primary treatment, as these cases often require a more extensive reconstruction to relieve intracranial pressure and reshape the skull. However, in select cases, an endoscopic procedure may be used as a first-stage surgery to relieve pressure before a more extensive reconstruction is performed later in childhood.

Another important consideration is parental commitment to helmet therapy. Unlike traditional surgery, where the surgeon immediately reshapes the skull during the procedure, endoscopic suturectomy relies on months of guided skull growth with a specially designed helmet. Families who are unable to commit to strict helmet therapy (23 hours per day for 6-12 months) may not see optimal results, making open surgery a more predictable option.

anterior cranioynostosis
Read More
Incidence

The overall incidence of Craniosynostosis is approximately 1 in 2000/3000 births. Lambdoid synostosis accounts for approximately 1% to 5% of all craniosynostosis cases.

Read More
Diagnosis

Diagnosis involves distinguishing lambdoid synostosis from positional plagiocephaly, a common condition caused by external pressure on the skull. Physical examination and imaging studies, such as CT scans, help differentiate between these conditions.

Read More
Treatment

Surgical treatment for lambdoid synostosis aims to correct the skull shape and alleviate any potential pressure on the brain. The procedure typically involves removing and reshaping the affected areas of the skull to achieve a more balanced and symmetrical appearance. Please refer to our Treatment Options page for a more detailed explanation of these surgical procedures.

Read More

Overview

Sagittal synostosis, also known as scaphocephaly, is the most common form of craniosynostosis. It involves the premature fusion of the sagittal suture, which runs from the front to the back of the skull along the midline. This fusion causes the head to grow long and narrow, a condition known as scaphocephaly.

Synostotic Anterior Plagiocephaly

Incidence

The overall incidence of Craniosynostosis is approximately 1 in 2000/3000 births. Sagittal synostosis accounts for approximately 40% to 55% of all craniosynostosis cases.

Diagnosis

Physical examination often reveals a long, narrow head shape with a prominent ridge along the sagittal suture. Confirmatory diagnosis is achieved through imaging studies such as CT scans, which provide detailed views of the fused suture and skull shape.

Treatment

Surgical treatment for sagittal synostosis aims to expand the width of the skull and improve its overall shape. Depending on the severity of the condition, procedures may include minimally invasive endoscopic suturectomy or a more complex procedure referred to as cranial vault remodeling. Please refer to our Treatment Options page for a more detailed explanation of these surgical procedures.

Making the Right Decision

Choosing the right treatment for craniosynostosis is a deeply personal decision that depends on your baby’s age, the severity of the condition, and your family’s commitment to following through with postoperative care. When diagnosed early, endoscopic suturectomy offers a minimally invasive way to correct craniosynostosis with less pain, a faster recovery, and excellent long-term results. However, for families seeking immediate correction without the need for helmet therapy, or for cases where the condition is more complex, cranial vault remodeling may be the better choice.

By working closely with a craniofacial specialist, you can determine whether your child is a good candidate for this approach and what to expect in the weeks and months following surgery. In the next sections, we will take a closer look at the preoperative evaluation process and the procedure itself to give you a clear understanding of what to expect throughout the process.

Endoscopic Suturectomy scaled

Preoperative Evaluation

Once a baby has been identified as a candidate for endoscopic suturectomy, the next step is a thorough preoperative evaluation. This stage ensures that the child is healthy enough for surgery, confirms the diagnosis and severity of craniosynostosis, and prepares both the medical team and parents for what to expect before, during, and after the procedure. Unlike open cranial vault surgery, which involves a more extensive reshaping of the skull, endoscopic suturectomy relies on early intervention and guided growth. Because of this, timing and careful planning are essential to achieving the best outcome.

A successful evaluation involves several key components, including a clinical examination, imaging studies, and coordination with a multidisciplinary team. You will also meet with your surgeon and other specialists who will be involved in your child’s care. This is an important time to ask any lingering questions, discuss the logistics of the surgery and helmet therapy, and ensure that your family is prepared for the process ahead.

Parental Preparation: What to Expect Before Surgery

In the days and weeks leading up to the procedure, you will receive specific instructions to help prepare your baby for surgery. These typically include:

The Endoscopic Suturectomy Procedure

On the day of surgery, you may feel a mix of emotions—hope, nervousness, and a strong desire to ensure your baby is receiving the best possible care. While endoscopic suturectomy is a minimally invasive procedure, understanding exactly what happens during surgery, how long it takes, and what to expect afterward can provide reassurance. Unlike traditional cranial vault remodeling, which involves extensive skull reshaping and longer recovery times, this approach focuses on removing the fused suture with minimal disruption to the surrounding bone, allowing the skull to reshape naturally with the help of helmet therapy.

This section will walk you through the entire surgical process—from arrival at the hospital to the procedure itself and the immediate recovery period. Knowing what to expect can help you feel prepared and confident as you support your child through this important step in treatment.

Arriving at the Hospital & Pre-Surgical Preparation

Step-by-Step Breakdown of the Surgery

Once your baby is fully asleep under anesthesia, the surgical team will proceed with the following steps:

 1.

Positioning & Sterilization

  • Your baby is carefully positioned, usually lying on their back, to provide the best access to the affected suture.
  • The surgical area is cleaned and sterilized, and a small portion of the hair may be shaved near the incision sites.

 2.

Creating the Small Incisions

  • The surgeon makes two or three small incisions (about 1-2 cm each) over the fused suture.
  • These incisions are made in locations that will heal well and be minimally visible over time.

 3.

Using the Endoscope for Visualization

  • A tiny, camera-guided instrument called an endoscope is inserted through one incision. This allows the surgeon to see the fused suture with high precision while keeping the incisions as small as possible.
  • Other small instruments are inserted through the additional incisions to carefully cut and remove the fused suture.

 4.

Removing the Fused Suture

  • Using specialized tools, the surgeon removes a strip of bone along the fused suture to create space for the skull to grow naturally.
  • The amount of bone removed is typically 1-2 cm wide, just enough to release the restriction without affecting surrounding areas.

 5.

Controlling Bleeding and Ensuring Safety

  • Since the incisions are small, bleeding is usually minimal, but the surgeon takes extra care to seal small blood vessels as needed.
  • The dura (the protective layer around the brain) is carefully preserved, and the skull is left intact aside from the removed suture.

 6.

Closing the Incisions

  • The surgeon closes the small incisions using dissolvable stitches or surgical glue. These will heal on their own over the next few weeks.
  • No plates, screws, or artificial implants are needed, as the skull will reshape naturally with helmet therapy.

Immediate Postoperative Recovery

After surgery, most babies wake up within 30-60 minutes in the postanesthesia care unit. Parents are usually brought in as soon as their baby starts waking up and responding. It’s common for babies to feel groggy, fussy, or slightly disoriented, but this is temporary and improves as the anesthesia wears off. Here are a few details about the most commonly asked questions about recovery

Helmet Therapy & Postoperative Management

The success of endoscopic suturectomy does not end in the operating room. Unlike traditional open surgery, where the skull is reshaped immediately, this minimally invasive approach relies on the baby’s natural growth to gradually correct head shape. Helmet therapy plays a critical role in ensuring the best possible cosmetic and functional outcomes.

Helmet therapy can feel like a big commitment—it requires consistent wear (23 hours per day) for several months and regular adjustments. However, when used correctly, it allows for a smooth and even expansion of the skull, helping the baby’s head grow into a normal, symmetrical shape. This section will explain how helmet therapy works, what to expect, and how to ensure the best results in the months following surgery.

Why is Helmet Therapy Necessary?

What happens after endoscopic suturectomy?

After endoscopic suturectomy, the removed suture leaves a gap, allowing the skull to grow in previously restricted areas. However, without guidance, the
head may not expand evenly. The helmet provides a gentle but structured shape, ensuring that as the skull grows, it fills in the right areas while preventing unwanted flattening or irregularities.

Why Helmet Therapy is important?

Helmet therapy is especially important because babies’ skulls grow the fastest in the first year of life, meaning this is the ideal time to reshape the head naturally without additional surgery. Parents who are diligent about keeping their baby in the helmet for the recommended time typically see excellent results, often resulting in a near-normal head shape by the child’s first birthday.

Getting Started

Outcomes & Long-Term Results

For parents choosing endoscopic suturectomy, one of the most important questions is: What kind of results can we expect? The good news is that this minimally invasive approach provides excellent cosmetic and functional outcomes when performed early and followed by consistent helmet therapy.

Unlike traditional open surgery, which reshapes the skull immediately, endoscopic suturectomy allows the baby’s natural growth to do most of the work. As a result, improvements become more apparent over time, with the most significant changes occurring within the first 12-18 months after surgery. By the time treatment is complete, most children have normal or near-normal head shapes and no long-term functional issues related to craniosynostosis.

Getting Started

Comparing Endoscopic Suturectomy and Cranial Vault Remodeling

For parents exploring treatment options for craniosynostosis, one of the biggest decisions is choosing between endoscopic suturectomy and traditional CVR. Both surgeries aim to correct skull shape abnormalities and facilitate normal brain growth, but they take very different approaches.

Endoscopic suturectomy is minimally invasive, relying on early intervention and helmet therapy to guide natural skull growth. Cranial vault remodeling, on the other hand, is a more extensive procedure that immediately reshapes the skull and does not require helmet therapy afterward. Each approach has its advantages, challenges, and ideal candidates, making it important for parents to understand which option best suits their child’s needs.

Key Differences Between Endoscopic Suturectomy & Cranial Vault Remodeling

FeatureEndoscopic SuturectomyCranial Vault Remodeling (CVR)
Age RequirementPerformed before 3 months of agePerformed between 6–12 months
Surgical ApproachMinimally invasive (small incisions)Open surgery (large incision across the scalp)
Procedure TimeAbout 1 hour3–5 hours
Blood LossMinimal, low chance of transfusionHigher blood loss, higher chance of transfusion.
Hospital Stay1 day or overnight3–5 days
Recovery TimeFaster, minimal swellingLonger, significant swelling
Helmet Therapy?Required for 6–12 monthsNot required
Results TimelineGradual improvement over timeImmediate reshaping
Ideal case severityMild to moderate casesModerate to severe cases
Long-Term OutcomesExcellent if helmet therapy is followedExcellent, no helmet needed

Both procedures are suitable for treating craniosynostosis. The choice often depends on the child’s age at diagnosis, the severity of the skull deformity, and the family’s ability to commit to postoperative care.

Advantages of Endoscopic Suturectomy

Immediate skull reshaping

The skull is fully corrected in the operating room, so parents see results immediately.

Better for severe cases

If the skull deformity is more complex, CVR allows for a more dramatic correction.

Less reliance on post-op compliance

Since results are achieved during surgery, families do not have to worry about helmet therapy adherence.

Downsides of CVR

The main downside of cranial vault remodeling is that it is a more invasive procedure, causing more swelling and requiring a longer hospital stay and recovery. However, for babies who are not eligible for endoscopic surgery due to age or case severity, it remains the gold standard for craniosynostosis correction.

Advantages of Cranial Vault Remodeling (CVR)

Immediate skull reshaping

The skull is fully corrected in the operating room, so parents see results immediately.

Better for severe cases

If the skull deformity is more complex, CVR allows for a more dramatic correction.

Less reliance on post-op compliance

Since results are achieved during surgery, families do not have to worry about helmet therapy adherence.

Downsides of CVR

The main downside of cranial vault remodeling is that it is a more invasive procedure, causing more swelling and requiring a longer hospital stay and recovery. However, for babies who are not eligible for endoscopic surgery due to age or case severity, it remains the gold standard for craniosynostosis correction.

Which Procedure is Best for Your Child?

The Baby’s Age

  • Under 3 months: Endoscopic suturectomy is an option (if helmet therapy is feasible).
  • Over 6 months? → Cranial vault remodeling is likely the better choice.

The Severity of the Skull Deformity

  • Mild to moderate craniosynostosis: Endoscopic suturectomy may work well.
  • Severe skull distortion? → Cranial vault remodeling offers a more immediate and controlled correction.

Parental Preference & Commitment to Helmet Therapy

  • Families who are comfortable with long-term helmet therapy often prefer endoscopic surgery.
  • Parents who want immediate results and minimal follow-up care may choose CVR.

Who will guide this decision?

  • A craniofacial surgeon will help guide this decision, taking into account your child’s specific condition, your preferences, and the expected long-term results.

Parental Perspective: What Do Families Say About Their Experiences?

Parents who choose endoscopic suturectomy often appreciate the quick recovery, minimal scarring, and lower surgical risks, but they also emphasize the importance of commitment to helmet therapy. Some families initially express concerns about the helmet but later find that their baby adjusts quickly, and they are thrilled with the final results.

On the other hand, parents who choose cranial vault remodeling often feel relieved to have a one-time surgery with no follow-up helmet therapy. Many families appreciate seeing the immediate correction in their child’s head shape and feel reassured that no further interventions will be needed.

Both procedures have high success rates, and ultimately, most families feel confident in their choice once they see their child’s progress.

Complications and Challenges

No matter how advanced a surgical procedure is, every operation carries some degree of risk. Fortunately, endoscopic suturectomy is considered very safe, with a low complication rate compared to traditional open surgery. However, like any medical procedure, it does have potential risks and challenges that you should be aware of.
Understanding possible complications, how they are managed, and what signs to look out for during recovery can help you feel more prepared and confident in your child’s treatment plan. While the vast majority of babies recover smoothly without issues, knowing what to expect can make the experience less stressful and allow you to take quick action if concerns arise.

Challenges Parents May Face

While medical complications are rare, parents may encounter challenges related to the recovery process, helmet therapy, and emotional aspects of treatment.

Future Directions & Innovations in Craniosynostosis Treatment

Medical advancements are constantly improving the diagnosis and treatment of craniosynostosis. While endoscopic suturectomy has revolutionized early treatment, ongoing research and new technologies continue to push the field forward, aiming for even safer, more effective, and less invasive options.

From advancements in surgical techniques to improved helmet therapy designs and potential nonsurgical interventions, the future of craniosynostosis treatment looks promising. Parents considering treatment can feel confident that they are benefiting from cutting-edge medical care, and future generations may have even more refined options available.

laughing mother lifting her adorable newborn baby son air scaled

Key Takeaways

Craniosynostosis is treatable

With early intervention, either through endoscopic suturectomy or cranial vault remodeling, most children achieve excellent outcomes, with normal skull growth and development.

Timing matters

Endoscopic suturectomy is most effective before 3 months of age, while cranial vault remodeling is better suited for infants 6-12 months old or those with more severe skull deformities.

Helmet Therapy is essential for endoscopic surgery

Helmet therapy is essential for endoscopic surgery. The success of endoscopic suturectomy depends on consistent helmet wear (23 hours per day for 6-12 months) to guide proper skull growth.

Choosing Endoscopic Suturectomy or Cranial Vault Remodeling

Whether choosing endoscopic suturectomy or cranial vault remodeling, both procedures have excellent long-term results with minimal risk of complications when performed by an experienced craniofacial team.

There are minimal long-term effects

There are minimal long-term effects. Once treated, most children experience normal brain development, engage in physical activity, and lead their daily lives with no restrictions or ongoing medical concerns.

Support is available

Parents don’t have to navigate this journey alone—there are craniosynostosis support groups, online communities, and medical professionals who can help every step of the way.

Actionable Steps for Parents

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