Bicoronal synostosis is a condition where both the coronal sutures of the skull (Growth plate between frontal and parietal bones) fuses early. The coronal sutures usually fuse in adulthood. In Bicoronal synostosis, the sutures fuse before birth.
This results in a flat head shape, also called as Brachycephaly.
This condition is quite common. Apert syndrome is one of the common syndromic craniosynostosis which is associated with Bicoronal craniosynostosis.
The main consequences of Bicoronal synostosis are:
Cranial index is the proportion of Bi-parietal diameter (BPD) to the Antero-posterior diameter (APD).
BPD is measured from the widest part of the skull - Side to side.
APD is measured from the longest part of the skull - Front to back
Normal Cranial Index is between 75-85.
Anything below 70 is Scaphocephaly and anything above 90 is Brachycephaly.
Bicoronal synostosis requires surgery for complete correction. Our protocol is as follows:
Non-syndromic
Age below 6 months - Endoscopic strip craniectomy & Orthotic Helmet Therapy
Age above 6 months - Fronto orbital advancement remodelling
Syndromic
Posterior vault expansion using Springs
Fronto orbital advancement remodelling
Timing depends on a case to case basis
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