Open access peer-reviewed chapter - ONLINE FIRST

Craniofacial Corrective Surgery in Syndromic Craniosynostosis

By Khairul Bariah Chi Adam, Firdaus Hariri, Wei Lee Chee, Kathiravan Purmal, Mohd Faizal Abdullah and Nazer Berahim

Submitted: June 30th 2020Reviewed: October 21st 2020Published: November 30th 2020

DOI: 10.5772/intechopen.94584

Downloaded: 66


This surgical field has now progressed and becoming an established subspecialty involving various surgical disciplines worldwide. Various complex CMF syndromes reported in syndromic craniosynostosis include Crouzon, Apert and Pfeiffer syndromes. These syndromes carry specific functional discrepancies associated with the affected structural anomaly and may therefore have functional issues involving the brain, eye and airway among others. As corrective surgery is often indicated depending on the affected vital functions, other factors that need to be considered are patient’s age, comorbidities, urgency, available expertise and patient’s overall prognosis based on the degree of anomaly. As such, the corrective surgery can be categorized into; (1) intermediate which is performed at an early phase and aimed to improve or salvage important vital functions such as the brain, eye, airway or feeding which are important for the child’s development and, (2) definitive treatment aimed at permanently correct the functional discrepancies. Intermediate corrective surgery may include invasive procedures such as ventriculo-peritoneal (VP) shunts, tarsorrhaphy, adenotonsillectomy and tracheostomy whereas definitive corrective surgery may include surgical procedures such as monobloc, Le Fort III osteotomy, posterior cranial vault expansion and mandibular advancement. This chapter will elaborate on the indications, types, challenges in the management and the proposed prevention measures in corrective surgery for specifically for syndromic craniosynostosis patients.


  • corrective surgery
  • syndromic craniosynostosis
  • craniofacial surgery

1. Introduction

Syndromic craniosynostosis is a condition which involves premature fusion of multiple skull sutures and may be associated with extracranial deformities such as limb, cardiac and tracheal malformations [1, 2]. Therefore, this syndrome usually comes with related issues such as increased intracranial pressure which can cause visual impairment (increased intraocular pressure), sleep impairment and eating difficulties due to midface hypoplasia, and even risk of impairment of mental development [3]. There are about 150 syndromes associated with craniosynostosis namely Crouzon, Pfeiffer and Apert syndrome.

Therefore, corrective surgery in syndromic craniosynostosis were developed in relation to its deformities and functional issues. Conventional craniofacial surgical techniques, such as strip craniectomy, fronto-orbital advancement, and Le Fort III procedures proved to be reliable to treat symptomatic syndromic craniosynostosis. However, limitations were observed in severe conditions where large segmental advancement were required, difficulty to close the gap primarily as well as inadequate stability secondary to soft tissue restriction and unstable bone segment fixation. These limitations thus causing relapse and creating less than an ideal long-term outcome [4]. Hence distraction osteogenesis (DO) were introduced to provide a reliable surgical alternative in achieving superior segmental advancement compared with conventional techniques in treating functional issues in syndromic craniosynostosis.

Syndromic craniosynostosis patients usually presented with multiple major functional disturbances which requires multi-disciplinary management including maxillofacial surgery, neurosurgery, plastic surgery and ENT among others. As such, the indication for each major surgery in paediatric patients with this condition should be discussed by the craniofacial team members as the procedure carries substantial mortality and morbidity risks [5].

2. Syndromic craniosynostosis and the genetic perspectives

Craniosynostosis was first known as craniostenosis that was introduced by German pathologist, Virchow in 1851. It was then changed to craniosynostosis and widely accepted ever since [6]. Craniosynostosis is a condition whereby the process of early or premature fusion of the skull sutures happens that leads to the unwanted growth pattern of the skull. The skull will not be able to grow perpendicular to the fused suture but instead will grow in parallel direction to the fused suture. The brain will use the space available to grow and cause an abnormal head shape and facial features [7]. In cases whereby the skull does not have any spaces due to fused sutures, the brain will continue to grow thus causing increased in intracranial pressure hence patient will develop visual disturbances, sleeping impairment due to airway disruption, eating difficulties because of unusual jaw growth and reduction in mental development.

Most known craniosynostosis cases are nonsyndromic and can occur as an isolated event or associated with other skeletal and developmental anomalies in specific clinical features for recognized syndromes. Patients who have been diagnosed with syndromic craniosynostosis are much more complex and require a multidisciplinary approach to effectively manage all the problems faced. Most of the syndromic craniosynostosis cases are due to genetic defect that may present as autosomal dominant, autosomal recessive and X-linked patterns of inheritance. The molecular genetic protocol for the diagnosis of syndromic craniosynostosis such Crouzon syndrome includes first-line tests of FGFR2 exons IgIIIa and IgIIIc followed by second-line tests of FGFR2 exons 3, 5, 11, and 14 to 17 and FGFR3 Pro250Arg and Ala391Glu as proposed by Wilkie et al. [7]. There are multiple types of syndromic craniosynostosis cases but almost all of the them shared the same craniomaxillofacial features such as exophthalmos, midface hypoplasia, cranial base anomalies as well as abnormal face with the additional limb anomalies [8, 9]. Syndromic craniosynostosis occurs in 1:8750 newborns [10, 11, 12, 13]. The most common syndromic craniosynostosis cases identified and managed are Crouzon, Apert, and Pfeiffer syndromes. These syndromes may be presented with identical craniomaxillofacial features. Therefore, it is prudent to differentiate to achieve an accurate diagnosis by relating to other features such digital or limb anomalies.

2.1 Crouzon syndromes

Clinically, patients may present with brachycephaly, small or shallow orbits with exophthalmos, midface hypoplasia and occlusal anterior open bite. However, there are no recorded cases that anomalies involving limbs are present. It is an autosomal dominant inheritance pattern that showed mutations in the fibroblast growth factor receptor 2 (FGFR-2) and occurred in 1 in 25,000 live births thus the most common syndromic craniosynostosis identified. Patients who have been diagnosed often have normal intelligence. Several cases identified as higher risk of increased intracranial pressure compared to other syndromic craniosynostosis cases [8, 14, 15]. The most common synostosis pattern observed is bicoronal synostosis which leads to brachycephalic shape, others such as scaphocephaly, trigonocephaly and cloverleaf skull have been diagnosed. Early fusion of cranial sutures resulted in shallow orbits and eye proptosis, small & high arched palate and anterior open bite. Eye proptosis or exorbitism can cause exposure conjunctivitis, keratitis, visual acuity problems and herniation of the globe. The synostosis will lead to midface hypoplasia as well and with normal development of mandible, class III skeletal profile & malocclusion formed. There are also other conditions reported such conductive hearing deficit, strabismus and hydrocephalus.

2.2 Apert syndromes

Often patients will present with turribrachycephaly, midface hypoplasia, symmetrical syndactyly of both hands and feet. It is also an autosomal dominant inheritance pattern with mutations in FGFR-2 occurring in 1 in 100,000 births with cases seen are sporadic new mutations. Bicoronal synostosis with large anterior fontanelle, bitemporal widening and occipital flattening is common presentation in most patients. In this syndrome, the midface hypoplasia is more severe than others with concavity of the face, very shallow orbits, mild hypertelorism and downslanting palpebral fissure, eye proptosis, cleft palate, anterior open bite. It will have the characteristic depressed nasal bridge and downward tip resulting in parrot beak deformity. The severe hypoplastic midface in Class III skeletal features will result in a small airway that causes airway compromise needing a tracheostomy to secure the airway.

Pathognomonic syndrome will be the hand syndactyly which often involve fusion of the second, third and fourth fingers that lead to middigital hand mass with the first and fifth fingers may also join. In certain cases, if the thumb is free, it is broad and deviates radially. In the feet, syndactyly will involve the second, third and fourth toes. Patients will suffer loss of function and referral to a hand surgeon is essential. Many patients have normal intelligence despite of some cases delayed mental development identified. Marruci et al. published the Great Ormond Street Hospital data on the expectant management of their patients in raised ICP in Apert syndrome. Their protocol is to offer cranial vault expansion only in the setting of confirmed elevation of ICP. Raised ICP developed in 83% of patients, 50% in the first year of life with the average age at onset was at 18 months. 35% of those treated successfully for their first episode however, went on to develop a second episode on average 3 years 4 months later [16].

2.3 Pfeiffer syndrome

Characterized by features of craniofacial anomalies from mild to severe condition. It includes turribrachycephaly, midface hypoplasia, exorbitism and the pathognomonic features of broad thumbs and great toes with variable soft tissue syndactyly. Other associated features include hypertelorism, strabismus, downslanting palpebral fissures, class III malocclusion and beaked nasal deformity. Again, the majority of cases involve FGFR-2 mutations, 5% of patients express an FGFR-1 mutation and demonstrate less severe phenotype [17, 18]. It is an autosomal dominant inheritance pattern with the incidence of 1 in 100,000 births. A classification system proposed that patients are categorized into three types based upon clinical findings and severity. Type 1 is the classic Pfeiffer syndrome clinical pattern. Type 2 is more severe and associated with the cloverleaf skull and type 3 Pfeiffer syndrome is the most severely affected. In one institution, a review of 28 patients has been conducted and the Cohen subtypes dissemination is 61% type 1, 25% type 2 and 14% type 3 [19]. All patients have undergone numerous corrective surgery. This study recommends aggressive treatment and monitoring on patients’ functional conditions to prevent further damage to the vital organ that leads to permanent loss of function.

Therefore, syndromic craniosynostosis is a condition of multiple associated clinical problems with the same pattern of treatment strategies, expected difficulties and pathologic identifications. Profound knowledge of the disease process, pathognomonic findings and clinical situations of each syndrome is essential. Therefore, multidisciplinary approach in total management of the clinical problems is important and must be detected and treated earlier to improve patient’s functional conditions and quality of life.

3. Corrective surgery

3.1 Pre-surgical assessment & preparation

In syndromic craniosynostosis, surgical intervention is often functionally indicated with the primary aim is to treat the pressing functional discrepancy or to salvage vital structures such as the brain and eyes [4, 20]. The three main functional issues secondary to the severe skull deformity are increased intracranial pressure, severe exopthalmos and obliterated nasopharyngeal airway. As such, comprehensive assessment to the brain, eyes and upper airway is paramount to determine the specific problem prior to any surgical decision.

3.1.1 Multi-disciplinary approach

Taking the multiple functional issues into consideration, multi-disciplinary approach has become the trend in syndromic craniosynostosis management. A craniofacial centre or unit may consist of various specialties such as neurosurgery, oral and maxillofacial surgery, plastic surgery, otorhinolaryngology, ophthalmology, and oculoplastic, among others.

3.1.2 General assessment

Patient growth progress and development should be assessed and properly documented as it provides valuable baseline and comparative data before and after surgery. This includes objective data such as head circumference, height, weight, gross and fine motor, as well as speech development, among others. These parameters are important as it may determine whether any corrective surgery should be indicated as early as possible or performed at a later stage [21].

3.1.3 Clinical assessment

Specifically on the craniofacial region, assessment can be focused on patient’s initial head shape, the degree of exopthalmos, ability for eyelid closure, nasal airflow, midfacial projection, jaw relationship and intraoral condition. Clinical picture documentation is very useful as it can be used for serial comparison.

3.1.4 Imaging assessment

Imaging modalities provide valuable input in identifying a specific functional issue. Magnetic resonance imaging (MRI) or CT scan may indicate any anomaly in the brain region and the condition of skull bone, respectively. Thinning of bone or copper beaten appearance is an indication to raised intracranial pressure necessitating corrective surgery to improve the intracranial volume via procedures such as posterior vault expansion or fronto-orbital advancement as shown in Figures 1 and 2.

Figure 1.

Thinning of the skull bone noted from the reconstructed 3D CT scan.

Figure 2.

Surgical simulation on the monobloc advancement of the frontofacial segment.

3.1.5 Ophthalmological assessment

Specific ophthalmological assessment such as retinal camera or fundoscopy provides information of the interior surface of the eye, including the retina, vasculature, optic disc and macula. Pale disc may be an indication of increased intracranial pressure. Tonometry can be performed to measure the intraocular pressure. Assessment of the volume of eye sockets is also important and can be conducted via the analysis of CT scan.

3.1.6 Airway assessment

For the airway, endoscopic examination is often performed to determine the cause of airway obliteration. The cause can either be due to soft tissue or hard tissue or both. Specific recognition of the anatomical restriction allows the surgical team to decide on the most ideal corrective surgical intervention such as shown in Figure 3. As most syndromic craniosynostosis patients are classically presented with midface hypoplasia, polysomnography (PSG) is the gold standard to diagnose obstructive sleep apnea (OSA).

Figure 3.

Airway assessment using software and CT scan.

3.1.7 Pre-operative preparation

Other pre-surgical preparation includes patient optimization prior to surgery via comprehensive in ward assessment by paediatric respiratory physician and anaesthetist.

Patient’s CT image can be used for surgical simulation using surgical software and utilized for 3D model fabrication to optimize the corrective surgery outcomes as shown in Figure 4. The technology provides precision and significantly reduces the operating hours thus minimizing the potential complication such as intra-operative bleeding [21, 22, 23, 24]. All patients in the authors’ center had their 3D skull bio-model fabricated to allow surgical simulation and vector determination to optimize the outcome of surgery. The pre-bending of the distractor footplates for the internal device and presurgical simulation proved critical because it contributed to the precision of device fixation and correct segmental movement to ensure a favorable final outcome and decrease operating time.

Figure 4.

Simulation of the surgical procedures using reconstructed 3D STL model from the CT scan.

The selection of devices is based on device suitability and functional indications. Increased ICP was assessed by history, presence of signs or symptoms, imaging analysis, and ophthalmologic assessment. For the eye, the patients’ ability to achieve eyelid closure was assessed and documented and supplemented with eye examinations that included optic disc condition and cup-to-disc ratio through funduscopy. Airway function was assessed by polysomnography and digital airway assessment.

Intra-operative complications should be anticipated thus preparation should include paediatric intensive care unit booking, blood cross-matched and reserve for transfusion as well as appropriate drug prescription.

When certain corrective surgery has been agreed by the multi-disciplinary team, consent should be clear and comprehensive with consideration of various complications ranging from mild to severe degree, at intra-operative and post-operative phase.

3.2 Surgical techniques and its application

Following comprehensive assessment from the craniofacial team, the choice of surgery basically depends on the aim, condition of the patient, skill of the surgeons and the facility. Hariri et al. [25] proposed for a protocol to indicate the type of intervention based on the aim of the functional rehabilitation. The protocol explained on the extend of surgical treatment depending on the patient’s severity, age as well as whether it can be done in stages or in combination to address the issues.

In multiple aims for rehabilitation in very young patient for example, increased ICP with hydrocephalus would necessitate less extensive surgical intervention such as ventriculoperitoneal (VP) shunting, while severe orbital proptosis might indicate temporary tarsorraphy, and respiratory difficulty would necessitate a continuous airway pressure device, a nasal stent, or a tracheostomy depending on the severity and the specific anatomic obstruction. More extensive surgical procedures are usually deferred up to certain age to reduce possibility of complications.

3.2.1 Posterior vault distraction/expansion

Posterior cranial vault expansion is usually indicated in increased in ICP cases without other functional issues when the patient’s age is more suitable [26, 27]. The aim is to increase the cranial volume to accommodate for the brain growth whilst reducing the intra cranial pressure.

3.2.2 Fronto orbital advancement & Monobloc Le Fort III advancement

Increased ICP with orbital proptosis might require fronto-orbital advancement with or without cranioplasty, and increased ICP in the presence of orbital proptosis and hypoplastic maxilla might require a monobloc as practiced in the authors’ center. Surgery can be performed conventionally or combined with distraction osteogenesis (DO) technique, which is indicated for superior structural expansion and achieving simultaneous new histogenesis compared with conventional surgical procedures [28]. The application of DO in treating craniofacial deformity was first reported in 1992 [29]. Since then, the benefits of this technique in treating syndromic craniosynostosis as reported in the literature are similar to those in the present study, which include marked improvements in functional parameters involving eye protection, preventing the increase of ICP, and treating airway deficiency [30, 31, 32, 33, 34].

3.2.3 Le Fort III osteotomy

Le Fort III advancement is aimed on improving the proptotic condition as well as opening the space for the upper airway. Syndromic craniosynostosis patients may presented with restricted upper airway thus causing obstructive sleep apnoea and shallow orbital floor. This allows the floor of the orbit to be advanced while opening the upper airway region on the nasal and maxillary region. This technique can be performed via conventional advancement or via DO depending on the amount of advancement and the experience of the team.

3.2.4 Le Fort I osteotomy

This is usually indicated in a later stage when the patient is more stable in growth to correct skeletal discrepancies such as retruded maxilla thus causing OSA. Therefore, the maxilla is advanced to gain space for airway. This procedure may be combined with other soft tissues surgery to gain optimum results in opening the airway such as tonsillectomy and adenoidectomy.

4. Complications

Craniofacial surgery is one of the established multidisciplinary specialty to produce safe surgery and good surgical outcome whilst minimizing the complications following surgical intervention for syndromic craniofacial patients. Although the results can be satisfying and there is general agreement on surgical indications, the potential remains for unwanted complications. The craniofacial surgery is unique because it involves exploration of the areas that allow very little margin of error. An inadequate knowledge of the anatomy, lack of training and surgical expertise can lead to not only disastrous results but even to the death of the patient. Any team that cares for craniofacial patients must take steps to avoid potential complications and be ready to deal with postoperative complications. Development of craniofacial surgery pioneered by Paul Tessier was a crucial step towards the paradigm shift in treating major craniofacial syndromic deformities [35].

4.1 Mortality and morbidity rate following craniofacial surgical intervention

The complications are the events that occurs during the management of craniofacial syndromes patients and may associated with any permanent deleterious effect on the patient. However, unfavourable outcomes generally are unexpected by the patients or surgeons [36].

The platinum rule to avoid any unwanted complications in any performed surgical procedures is to follow the dictum “Primum Non Nocere”.

Many authors attempted to classify the complications of craniofacial surgery that arise during intraoperative and postoperative, but these complications might differ with different craniofacial syndromes. Intraoperative and post-operative complications pertaining to cranial vault surgery was described and classified into early, immediate post-operative and late postoperative complications [37, 38, 39, 40, 41, 42]. Given the uniqueness presentation of patients with craniofacial syndromes, each patient presented with their own problems and complications following surgical intervention might be different from each other thus the need for comprehensive classification systems.

One of the easiest way to classify the complications following surgical intervention are by Sharma et al. 2013 [41] which was divided into four types:

Type 1: Minor events without any damaging effects on the patient. They include minor wound infections, poorly placed scars, minor cerebrospinal fluid leaks, and seromas/hematomas. Most of the time, this classification refers to less serious and minor complications following craniofacial surgery that consists of:


This is most of the time seen after hypertelorism correction but the reported incidence is quite low which is about 0.6% [42]. This is due to any procedure that involves dissection around the medial and inferomedial orbital floor may potentially damage the lacrimal drainage system.

Lateral canthal ligament dystopia

Extensive stripping of periorbita may lead to reattachment of periorbita at low level eventually resulting in enhanced antimongoloid slant. This is most frequently seen on syndromic rather than nonsyndromic craniofacial syndrome [22].

Hardware issues

Hardware can be considered as a foreign body thus occasionally can be infected, exposed or even palpable postoperatively. Infection and exposure of fixation material are rare in paediatric cranial vault surgery [42]. Metal fixation carry a possibility of intracranial fixation due to appositional cranial growth. Some reported translocation of hardware into calvarial bone in 14% and 6.6% with intracranial translocation and commonly occur in younger and syndromic patients [28]. Therefore, usage of resorbable hardware has now become more popular due to concerns about constriction of growth by metal fixation and the possibility of implant translocation [29, 30, 31, 32].

Bone graft donor morbidity

Pneumothorax incidence of 3% after rib harvesting in their experience but emphasized that the rates vary from 5–30% in other series [33].

Type 2: Moderate-to-severe events that compromise the results and might need another surgical intervention for a successful outcome. They include exposure keratitis, diplopia, contour deformities, warping, non/malunion, and exposed hardware.

Strabismus and temporary ptosis are frequently seen after cranial vault procedures that involve periorbita stripping [37]. McCarthy et al. noted preoperative strabismus in hypertelorism cases, which often worsened after surgery then stabilized approximately 6 months after surgery [38].

Cerebrospinal fluid (CSF) leak following craniofacial surgery and sequalae of neurosurgical infection is common. Obvious risk for infection with CSF was noted but also associated with impairment of wound healing. Predisposing factor that might lead to easy tear of dura are due to scar from previous surgery or abnormal bony contour with dural adhesion [36, 37, 38, 39]. Some tears may go unnoticed, and CSF may manifest postoperatively either as rhinorrhoea or leakage through the scalp wounds or within the drain itself.

Transient hyponatremia is one of the reported complications caused by secretion of inappropriate antidiuretic hormone (diabetes insipidus) has been reported [27, 40, 41, 42, 43, 44]. Researchers believe that it results from traction on the frontal lobes.

Unexpected airway issues are other complications following craniofacial surgery, in which emergency reintubation or even prolonged ventilation is needed due to severe upper airway oedema. Decision for steroid covers for upper airway oedema is most of the time anecdotal but some reported beneficial in preventing facial oedema postoperatively [45, 46, 47, 48, 49, 50].

Type 3: Serious events with unfavourable result which can or cannot be successfully managed. They include nerve palsies and infection leading to bone loss and partial loss of vision.

Infection is the most common complication in the form of osteitis/osteomyelitis, meningitis, or an intracranial abscess, occurring in 6.2% of transcranial cases [25]. Overall reported infection rates ranging from 1–14% in large centre series [27, 32, 39, 40, 41, 42, 47, 48, 49, 50, 51].

Permanent neurological deficit is another complication in craniofacial surgery that fall into type III classification. Majority of craniofacial surgery confined to extradural showed lower incidence of neurologic impairment. Several reports from major craniofacial centers has shown very low or no permanent neurologic deficits directly attributable to surgery [27, 30, 37, 50, 51, 52]. Blindness for example, is an unwanted complication in craniofacial surgery that post a real risk of blindness following surgery. Munro and Sabatier noted four cases of permanent blindness in 1092 procedures [54].

Type 4: Serious events that may even lead to death. They include postoperative infection, perioperative bleeding, respiratory compromise, or other serious anesthesia-related events.

Since 1970’s to 1988, rate of mortality in craniofacial surgery were reported ranging from 1 to 2% all over the world [47, 48, 49, 50, 51]. However, with development of the technology, deeper understanding of the craniofacial surgery and its risks with emphasis on multidisciplinary approach, the numbers of mortality have dropped to 0.1–0.8% in some centers [24, 25, 26, 27, 28, 29].

5. Research and development in corrective surgery

With the recent medical and technology advancement, patient management was more promising and in a well-controlled manner. The surgical management of craniosynostosis patient resurfaces again in the mid-20th century as a completely stand-alone surgical specialty. A more well defined surgical procedure, better anaesthetic protocols, together with the help of advanced technology, this group of patients now enjoy a safer surgical outcome [52, 53, 54, 55, 56, 57].

5.1 Optimal age of surgery

Surgical procedures advocated in this group of patients are aim to make sure normal growth of the brain and skull, and near to normal development to their adulthood. Controversy still on-going with the best timing of surgical intervention in this group of patients between early versus late surgical intervention. Early surgical intervention is always aiming for better corneal protection and to create spaces for constricted brain. Late surgical intervention conversely aiming for more stable bony correction and less likely for subsequent surgical intervention [50]. However, our center practice on more indication and need-based approach, surgical intervention at the best possible timing for patients in term of growing stage, the indication need for the surgery and patient’s general health condition [4].

5.2 Choices of osteotomy

Surgical procedures evolved from strip craniectomy, monobloc osteotomy, fronto orbital advancement and recently, posterior vault expansion. All these procedures are indicated to release the fused cranial suture, re-create more spaces for brain development and to make sure the bilateral eye globe is well protected as shown in Figures 5 and 6. The current treatment can be summarized in Table 1.

Figure 5.

Posterior vault distraction distraction osteogenesis indicated for only increased ICP with no other symptoms.

Figure 6.

Le Fort III advancement indicated for management of ICP, airway and orbital globe.

Issues to manageTreatment proposed
Only increase in ICPPosterior cranial vault distraction
Increase in ICP and shallow orbitFronto orbital advancement
Reduced airway and shallow orbitLe Fort III advancement
Reduced airway, shallow orbit and increased ICPMonobloc advancement

Table 1.

Treatment proposed for management of syndromic craniosynostosis issues.

Different surgeon will advocate different surgical technique at different timing, either with direct osteotomy and surgical plating or through distraction osteogenesis procedure [2, 4, 9, 49, 50, 58, 59]. There is no uniform surgical algorithm internationally, but more on surgeon or surgical center preferences. Obviously, these surgeries need collaboration of neurosurgeon, oral maxillofacial surgeon and otorhinolaryngologists.

5.3 Research

The ultimate goals for craniosynostosis treatment is mainly to restore function, improve facial aesthetic and ensure a healthy psychological development. More research is needed in this syndromic craniosynostosis in term of treatment algorithm, utilisation of latest and advancement of computer planning, computer navigation, 3-dimensional printing and usage of the cheaper, user friendly and effective surgical device in making the surgery more safer and more predictable outcome. The treatment focus not only on the fused suture of the skull, but also make an effort to address issue like intracranial pressure, strabismus, abnormally positioned orbit and dentofacial deformities [60, 61, 62]. Another area of future development will be in the molecular genetic testing in the field of genetic counselling.

6. Conclusions

Corrective surgery in syndromic craniosynostosis was formerly regarded as formidable however currently performed as a routine by major craniofacial center in the world due to advancement of technology and multidisciplinary approaches. Certain types of deformity, particularly those patients with Crouzon’s or Apert’s syndrome, require more than one functional intervention to achieve maximum correction.

In general, the surgical indication for paediatric CMF deformities can be classified into intermediate and definitive intervention. The intermediate intervention is performed at an early phase of patient’s life and aimed to salvage vital tissue or organ function such as the brain, eye, airway or feeding which are essential for the child’s development. The protocol of the management for syndromic craniosynostosis patients is summarized in Figure 7. These procedures include ventriculoperitoneal (VP) shunt, tarsorrhaphy, adenotonsillectomy and tracheostomy.

Figure 7.

Summary of indications for intervention in craniofacial syndromes.

Therefore, these interventions in craniofacial syndromes is associated with multiple morbidities. It is important to understand the need and risks of these interventions prior making decision of treatment for each patient. Craniofacial teams should be cognizant to audit data on morbidity and mortality as well as surgical outcomes to monitor complication rates.

Surgical risk stratification involving the severity of patient’s functional issues, age, co-morbidities, logistics, the timing and type of surgery and anticipated post-operative issues are in practiced to guide decision making consensus and serve as the index of precaution prior to any surgery [63]. This is in line with the recommendation of other centers which placed greater focus on protocols for airway management, blood salvage and replacement, age-appropriate deep venous thrombosis prophylaxis and timing of sub cranial midfacial advancements which might result in further reductions in craniofacial mortality rates.


We would like to thank everyone who were involved direct and indirectly in the making of this chapter, craniofacial team members, staff and patients in UMMC, HKL, and SASMEC@IIUM, Malaysia.

Conflict of interest

The authors declare no conflict of interest.

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Khairul Bariah Chi Adam, Firdaus Hariri, Wei Lee Chee, Kathiravan Purmal, Mohd Faizal Abdullah and Nazer Berahim (November 30th 2020). Craniofacial Corrective Surgery in Syndromic Craniosynostosis [Online First], IntechOpen, DOI: 10.5772/intechopen.94584. Available from:

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