(Q03.8) Other congenital hydrocephalus

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219 744 in individuals diagnosis other congenital hydrocephalus confirmed
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7 837 deaths with diagnosis other congenital hydrocephalus
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4% mortality rate associated with the disease other congenital hydrocephalus

Diagnosis other congenital hydrocephalus is diagnosed Men are 11.92% more likely than Women

122 967

Men receive the diagnosis other congenital hydrocephalus

4 022 (3.3 %)

Died from this diagnosis.

100
95
90
85
80
75
70
65
60
55
50
45
40
35
30
25
20
15
10
5
0
96 777

Women receive the diagnosis other congenital hydrocephalus

3 815 (3.9 %)

Died from this diagnosis.

Risk Group for the Disease other congenital hydrocephalus - Men and Women aged 0

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In Men diagnosis is most often set at age 0-59, 70-74
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Less common in men the disease occurs at Age 60-69, 75-95+Less common in women the disease occurs at Age 45-54, 75-84, 90-95+
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In Women diagnosis is most often set at age 0-44, 55-74, 85-89

Disease Features other congenital hydrocephalus

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Absence or low individual and public risk
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Other congenital hydrocephalus - what does this mean

Other congenital hydrocephalus is a condition that occurs when there is an abnormal accumulation of cerebrospinal fluid (csf) in the brain, resulting in increased pressure on the brain and skull. it can be caused by a blockage of the normal flow of csf, a structural abnormality of the brain or skull, or a genetic mutation.

What happens during the disease - other congenital hydrocephalus

Other congenital hydrocephalus is a condition in which cerebrospinal fluid accumulates in the ventricles of the brain due to an obstruction in the normal flow of the fluid. this obstruction can be caused by a variety of factors, including malformations of the brain, blockages of the ventricles, or infections of the central nervous system. the accumulation of the cerebrospinal fluid can lead to an increase in pressure within the brain, which can cause damage to the brain tissue and lead to a range of neurological symptoms.

Clinical Pattern

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How does a doctor diagnose

  • Neuroimaging (CT scan, MRI)
  • Neurological examination
  • Ultrasound of the head
  • Lumbar puncture
  • Genetic testing
  • Blood tests
  • Urine tests
  • Cerebrospinal fluid analysis
  • Electroencephalogram (EEG)

Treatment and Medical Assistance

Main Goal: To reduce hydrocephalus and improve the patient's quality of life.
  • Medication to reduce the production of cerebrospinal fluid
  • Surgical procedures to reduce the amount of cerebrospinal fluid
  • Regular monitoring of intracranial pressure
  • Physical therapy to help with motor skills
  • Occupational therapy to help with daily activities
  • Speech therapy to help with communication
  • Counseling to help with emotional and social issues
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18 Days of Hospitalization Required
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Average Time for Outpatient Care Not Established

Other congenital hydrocephalus - Prevention

Other congenital hydrocephalus can be prevented by avoiding exposure to certain environmental factors such as alcohol and drug use during pregnancy, maintaining good nutrition, and avoiding infections. additionally, regular prenatal care can help identify any potential risk factors and allow for early intervention if necessary.