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(Q01.8) Encephalocele of other sites
More details coming soon
26 067 in individuals diagnosis encephalocele of other sites confirmed
2 064 deaths with diagnosis encephalocele of other sites
8% mortality rate associated with the disease encephalocele of other sites
Diagnosis encephalocele of other sites is diagnosed Men are 5.43% more likely than Women
13 741
Men receive the diagnosis encephalocele of other sites
900 (6.5 %)Died from this diagnosis.
100
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12 326
Women receive the diagnosis encephalocele of other sites
1 164 (9.4 %)Died from this diagnosis.
Risk Group for the Disease encephalocele of other sites - 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 encephalocele of other sites
Absence or low individual and public risk
Encephalocele of other sites - what does this mean
Encephalocele of other sites is a rare congenital disorder in which the brain and/or its membranes protrude through an opening in the skull. it is usually caused by abnormal development of the neural tube during pregnancy, resulting in a defect in the skull that allows the brain or its membranes to herniate through. in some cases, the herniation may be large enough to cause a visible bulge on the head.
What happens during the disease - encephalocele of other sites
Encephalocele of other sites is a rare congenital disorder caused by a defect in the neural tube that occurs during the early stages of fetal development. this defect leads to the protrusion of brain tissue and/or meninges through a defect in the skull or face. this can result in a variety of neurological deficits, including cognitive and motor impairments, depending on the location and size of the defect.
Clinical Pattern
More details coming soon
How does a doctor diagnose
- Physical examination
- Neuroimaging, such as CT scan or MRI
- Cerebrospinal fluid analysis
- Electroencephalogram (EEG)
- Genetic testing
- Neuropsychological testing
- Angiography
Treatment and Medical Assistance
Main goal of the treatment: To reduce the risk of complications and improve the quality of life of the patient.
- Perform a surgical procedure to repair the encephalocele.
- Monitor the patient’s vital signs and neurological status.
- Administer antibiotics to prevent infection.
- Prescribe medications to reduce inflammation and reduce seizures.
- Administer physical therapy to improve strength, coordination, and balance.
- Provide nutritional support to help the patient heal.
- Educate the patient and family about the condition and its management.
- Refer the patient to a specialist for further evaluation and management.
16 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Encephalocele of other sites - Prevention
Encephalocele of other sites can be prevented by proper prenatal care, including regular check-ups, ultrasounds, and genetic testing. women should also take the necessary steps to prevent infections during pregnancy, such as avoiding contact with sick people, washing hands frequently, and avoiding certain foods and activities. vaccines can also help prevent some of the causes of encephalocele.