Premature fusion of coronal and sagittal sutures usually leads to a tall, tower-like skull which is known as turricephaly. Fusion of all sutures produces a tall pointed skull known as acro- or oxy-cephaly. Turri-, acro- and oxy-cephaly are associated with a CI of 80 or more. Individuals often have orbital protrusion secondary to shallow bony orbits. Almost half will have other anomalies and the risk of associated mental retardation is high (20-25%). Hydrocephaly occurs in 7% and optic atrophy due to increased intracranial pressure is not uncommon. The skull develops from mesenchyme, with the portion surrounding the brain termed the neurocranium. The neurocranium consists of a cartilaginous portion (chondrocranium) and a membranous portion. The chondrocranium is the cartilaginous base of the skull, which develops by fusion of several cartilages. The membranous neurocranium ossifies to form the cranial vault, the bones of which are separated by connective tissue membranes known as sutures. Six fibrous areas, the fontanelles, are also present. The five major sutures are the frontal, or metopic, sagittal, coronal, lambdoid and squamosal. The sutures allow for moulding to occur during the delivery process, and enlargement to accommodate normal brain growth. When the cranial bones fuse prematurely there is decreased growth potential. Bone deposition occurs abnormally, with the majority being directed away from the fused bony plate. In turn, perimeter sutures adjacent to the prematurely fused suture compensate in growth to a greater extent than sutures distant to the fused area. The primary cause of synostosis may be a defect at the cranial base at the site of initial attachment of the dura; other studies suggest a vascular defect causing deficient osteoclasia. Secondary craniosynostosis may occur because of brain abnormalities such as microcephaly or holoprosencephaly, or may be due to fetal constraint. Craniosynostosis has been reported to be present in 0.5 to 3.4 per 1000 live births. Sagittal synostosis accounts for 50%; coronal 22%; metopic 6%; and other or multiple 23%. Unilateral coronal synostosis is as common as bilateral. A predominance of males is noted, particularly for sagittal involvement. Craniosynostosis often causes alteration in head shape, ridging over the sutures, and/or fontanelle closure. Different terms have been used to describe the head shape alterations due to craniosynostosis, with resultant shape dependent upon the suture(s) involved.


Because sutures represent the boundaries of different cranial plates that are curvilinear, clear visualization of overall structural detail often is difficult. The diagnosis of craniosynostosis is generally made on the basis of abnormal cephalic index (CI), coupled with other features of unusual head shape which include increased vertical diameter of the skull, frontal bossing/ prominent forehead, flat face, proptosis/shallow orbits, hypoplastic nasal bridge, and abnormal eye measurements. These differences are best appreciated if the face is evaluated in all three planes – sagittal, coronal and transverse. The cephalic index (CI) is obtained using a transverse or axial image at the maximum dimensions of the head. Biparietal and fronto-occipital diameters are measured, in both cases from the outer margin of the calvarium to the opposing outer margin. CI = BPD/FOD x 100. Mean CI is 78.3%; SD is 4.4%. Values below 70 are interpreted to be indicative of dolichocephaly (or scaphocephaly), while values above 86 indicate brachycephaly. Three-dimensional visualisation based on volumetric ultrasonographic image data offers the possibility of revealing the structural coherence of the sutures and fontanelles in the fetal skull more clearly. This technique allows imaging of coronal, lambdoidal and squamosal sutures, anterior, posterior, mastoid and sphenoid fontanelles. Identification of craniosynostosis should lead to a detailed search for associated anomalies which, in particular, affect the limbs – short limbs, polydactyly and syndactyly.

Differential Diagnosis

Minor degrees of change in skull shape are part of the variation seen in the general population, and are not necessarily associated with craniosynostosis. This is particularly true of brachycephaly and dolichocephaly.

Sonographic Features

CI greater than 86 Increased vertical diameter of the skull

Flat face, shallow orbits

Unusual head shape

Associated limb anomalies include polydactyly, syndactyly, and short limbs


Associated Syndromes

  • Krassikoff
  • Pauli
  • Congenital hypothyroidism
  • Apert
  • Carpenter
  • Cutis gyratum-acanthosis
  • Elejalde
  • Kaplan
  • Osteoglophonic dysplasia


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Hadlock FP, Deter Rl, Carpenter RJ, Park SK Estimating fetal age: effect of head shape on BPD Am J Roentgenol 137: 83-5
Hill LM, Thomas ML, Peterson CS The ultrasonic detection of Apert syndrome J Ultrasound Med 6: 601-4
Narayan H, Scott IV Prenatal ultrasound diagnosis of Apert’s syndrome Prenat Diagn 10: 187-192
Parent P, Le Guern H, Munck MR, Thoma M Apert syndrome, an antenatal ultrasound detected case Genet Counselling 5: 297-301
Ashby T, Rouse GA, De Lange M Prenatal sonographic diagnosis of Carpenter syndrome J Ultrasound Med 13: 905-9
Nevin NC, Herron B, Armstrong MJ An 18 week fetus with Elejalde syndrome (acrocephalopolydactylyous dysplasia) Clin Dysmorph 3: 180-4
Cohen MM Jr Craniosynostosis update 1987 Am J Med Genet Suppl 4: 99-148
Pretorius DH, Nelson TR Prenatal visualisation of cranial sutures and fontanelles with three-dimensional ultrasonography J Ultrasound Med 13: 871-876