Non-syndromic sagittal craniosynostosis is a type of craniosynostosis, which is a condition in which the bones of the skull fuse together too early. In non-syndromic sagittal craniosynostosis, the sutures (the joints between the bones of the skull) fuse together in the midline of the skull, causing the head to become long and narrow. This condition is not associated with any other medical conditions or syndromes.

The most common symptoms of non-syndromic sagittal craniosynostosis include:

-A long, narrow head shape
-High forehead
-Widely spaced eyes
-Flattened back of the head
-Prominent occiput (back of the head)
-Crowding of the facial features
-Delayed motor development
-Delayed speech development
-Delayed cognitive development
-Sleep apnea
-Seizures
-Vision problems
-Hearing problems
-Hydrocephalus (buildup of fluid in the brain)

Non-syndromic sagittal craniosynostosis is a type of craniosynostosis, which is a condition in which the sutures of the skull close prematurely. The exact cause of non-syndromic sagittal craniosynostosis is unknown, but it is believed to be a combination of genetic and environmental factors. Genetic factors may include mutations in certain genes that are involved in the development of the skull, while environmental factors may include exposure to certain medications or toxins during pregnancy.

1. Cranial Vault Remodeling (CVR): This is a surgical procedure that reshapes the skull to allow for normal brain growth and development.

2. Endoscopic Strip Cranioplasty (ESC): This is a minimally invasive procedure that involves removing strips of bone from the skull to create a more symmetrical shape.

3. Cranial Reconstruction: This is a more complex procedure that involves reshaping the skull and reconstructing the bones to create a more symmetrical shape.

4. Cranial Distraction Osteogenesis (CDO): This is a procedure that uses a device to slowly separate the bones of the skull to create more space for the brain to grow.

5. Orthotic Therapy: This involves the use of a helmet or other device to help reshape the skull and encourage normal brain growth and

1. Family history of craniosynostosis
2. Premature birth
3. Low birth weight
4. Exposure to certain medications or drugs during pregnancy
5. Exposure to radiation during pregnancy
6. Maternal diabetes
7. Maternal smoking during pregnancy
8. Maternal alcohol consumption during pregnancy
9. Maternal obesity

Non-syndromic sagittal craniosynostosis is typically treated with surgery. The goal of the surgery is to reshape the skull and allow for normal brain growth. Medications are not typically used to treat this condition.