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(Q01.1) Nasofrontal encephalocele
More details coming soon
26 067 in individuals diagnosis nasofrontal encephalocele confirmed
2 064 deaths with diagnosis nasofrontal encephalocele
8% mortality rate associated with the disease nasofrontal encephalocele
Diagnosis nasofrontal encephalocele is diagnosed Men are 5.43% more likely than Women
13 741
Men receive the diagnosis nasofrontal encephalocele
900 (6.5 %)Died from this diagnosis.
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12 326
Women receive the diagnosis nasofrontal encephalocele
1 164 (9.4 %)Died from this diagnosis.
Risk Group for the Disease nasofrontal encephalocele - Men and Women aged 0
In Men diagnosis is most often set at age 0-24, 30-39, 65-74
Less common in men the disease occurs at Age 25-29, 40-64, 75-95+Less common in women the disease occurs at Age 20-24, 65-95+
In Women diagnosis is most often set at age 0-19, 25-64
Disease Features nasofrontal encephalocele
Absence or low individual and public risk
Nasofrontal encephalocele - what does this mean
Nasofrontal encephalocele is a rare congenital disorder that occurs when the bones of the skull fail to close completely, resulting in a sac-like protrusion of the brain and the membranes that cover it through the nose or forehead.
What happens during the disease - nasofrontal encephalocele
Nasofrontal encephalocele is a rare congenital abnormality caused by a defect in the closure of the neural tube during early embryonic development. this defect results in a protrusion of the brain and the covering of the brain (meninges) through an opening in the skull. this opening is typically located in the nasal region and can be associated with other craniofacial anomalies.
Clinical Pattern
More details coming soon
How does a doctor diagnose
- Physical examination of the patient
- CT scan of the skull
- MRI scan of the brain
- X-ray of the skull
- Ultrasound of the brain
- Angiography of the brain
- Genetic testing
Treatment and Medical Assistance
Main goal of the treatment: To reduce the size of the encephalocele and to prevent further complications.
- Provide supportive care to relieve symptoms
- Administer antibiotics to reduce the risk of infection
- Perform a craniotomy to reduce the size of the encephalocele
- Close the defect in the skull using sutures
- Prescribe medications to reduce swelling and inflammation
- Perform a CT scan to monitor the size of the encephalocele
- Provide nutritional support to ensure proper growth and development
16 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Nasofrontal encephalocele - Prevention
Nasofrontal encephalocele is a rare birth defect that can be prevented through proper prenatal care. this includes regular check-ups, folic acid supplementation, and avoiding alcohol and smoking during pregnancy. additionally, it is important to be aware of family history and any known genetic risk factors.