Both produce excellent cosmetic results with very low risk of complications. Additionally, the eye sockets may not grow laterally, giving the appearance that the eyes are too close together. • ICP or raised intracranial pressure caused due to the restriction of skull growth. The location where four of these large bones meet in the front of the head is called the anterior fontanelle, or soft spot (there is another one in the back of the head). Surgery The key to treating craniosynostosis is early detection and treatment. This surgery usually takes about 1 hour. Patient was discharged home the next day. Physical examination: The surgeon would look for facial deformities and feel the shape of your baby’s head for abnormalities like suture ridges. Learning that the baby may require craniosynostosis surgery can tend the parents to experience various emotions. This procedure involves removing the fused suture and strips of bone with an endoscope or lighted retractor through two small incisions. A procedure that can be performed on infants two months old or younger, or on babies nine to twelve months of age, Craniosynostosis surgery can correct the malformation of a child’s skull. Advantages include its minimally invasive nature, and reduced morbidity and hospital stay. It is estimated that this defect occurs in one out of every 2000 live births. Also, surgery is generally recommended to help these children have a normal head shape for self-esteem and social issues. Both produce excellent cosmetic results with very low risk of complications. The scope allows the surgeon to view the area being operated on. After the surgery, your child would require to wear a cranial orthotic helmet for some time to help mold the head into a normal shape as it grows. A craniosynostosis surgery is a reconstructive procedure to solve the problems mentioned above. Babies' heads come in all shapes and sizes. One month post Craniosynostosis surgery, my husband and I have plowed through Broxon's recovery with our heads down, hands together, and hearts full. Sagittal synostosis is the most common suture to close too soon, and it inhibits growth of the skull on both sides. A team of specialist surgeons having expertise in head, face and brain surgery is the best to perform Craniosynostosis surgery. Sometimes a craniofacial team coordinates the care of the child. Craniosynostosis is a birth defect of the head. It is a problem when the forehead becomes keel shaped (just like the front of a boat). Being a complex procedure, it typically involves the patient to stay in the hospital for about three to four days. Patients who had minimally invasive surgery may go home the next day. However, in Craniosynostosis, the skull bones of the infant fuse way too early and that can restrict the growth of the brain resulting in an abnormal shape of the head. Usually, the surgery is done by both a neurosurgeon and a plastic surgeon. Craniosynostosis is a rare condition where a baby's skull doesn't grow properly and their head becomes an unusual shape. It could be an open surgery or an endoscopic surgery depending on the patient’s condition. Patients are also required to wear a cranial-molding helmet for 7-9 months after surgery. Craniosynostosis is a birth defect in which one or more of the cranial sutures, or the joints between the bones of the skull, closes before the brain has completed growing. Usually, the surgery is done by both a neurosurgeon and a plastic surgeon. Usually, blood transfusion is also necessary. An x-ray or computed tomography (CT) scan can be used to diagnose craniosynostosis. It is not a problem when the only noticeable feature is a ridge on the forehead. The craniosynostosis Surgery procedure A team of specialist surgeons having expertise in head, face and brain surgery is the best to perform Craniosynostosis surgery. It is a one-time procedure, however, in complicated cases; several open-surgeries might be required to correct the shape of the baby’s head. Watch Craniosynostosis surgery procedure animation videos describing our newer, less invasive treatment. Most children after the craniosynostosis surgery achieve excellent cosmetic results and have normal cognitive development. Based on that virtual surgical plan, customized templates are constructed to guide the procedure. Not all patients are a candidate for all types of surgery. Among the limited number of patients who have had an endoscopic procedure, many have needed subsequent calvarial remodeling. 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