(Q06) Other congenital malformations of spinal cord

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51 463 in individuals diagnosis other congenital malformations of spinal cord confirmed
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1 311 deaths with diagnosis other congenital malformations of spinal cord
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3% mortality rate associated with the disease other congenital malformations of spinal cord

Diagnosis other congenital malformations of spinal cord is diagnosed Women are 0.62% more likely than Men

25 573

Men receive the diagnosis other congenital malformations of spinal cord

0 (less than 0.1%)

Died from this diagnosis.

100
95
90
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80
75
70
65
60
55
50
45
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15
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5
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25 890

Women receive the diagnosis other congenital malformations of spinal cord

1 311 (5.1 %)

Died from this diagnosis.

Risk Group for the Disease other congenital malformations of spinal cord - Men and Women aged 0-5

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In Men diagnosis is most often set at age 0-69, 75-79
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Less common in men the disease occurs at Age 70-74, 80-95+Less common in women the disease occurs at Age 75-95+
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In Women diagnosis is most often set at age 0-74

Disease Features other congenital malformations of spinal cord

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Absence or low individual and public risk
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Other congenital malformations of spinal cord - what does this mean

Other congenital malformations of the spinal cord occur when the spinal cord does not develop properly in the womb, either due to genetic or environmental factors. this can lead to a range of structural abnormalities, such as incomplete closure of the vertebral arches, abnormal vertebral segmentation, and abnormal curvature of the spine. these malformations can cause a range of neurological symptoms, including paralysis, sensory deficits, and motor deficits.

What happens during the disease - other congenital malformations of spinal cord

Other congenital malformations of the spinal cord are caused by abnormal development of the neural tube during early embryonic development. these malformations can involve the vertebrae, meninges, nerve roots, and spinal cord itself, and can result in a wide range of symptoms, including sensory and motor deficits, pain, and paralysis.

Clinical Pattern

More details coming soon

How does a doctor diagnose

  • Physical examination
  • Imaging studies such as X-ray, CT scan, MRI scan
  • Electromyography (EMG)
  • Ultrasound
  • Cerebral spinal fluid (CSF) analysis
  • Genetic testing
  • Neurological evaluation
  • Neuropsychological testing

Treatment and Medical Assistance

Main goal of the treatment: To reduce the severity of the symptoms and improve the quality of life of the patient.
  • Surgery to correct the malformation
  • Medication to reduce inflammation and pain
  • Physiotherapy to improve mobility and strength
  • Occupational therapy to improve daily functioning
  • Psychological support to manage stress and anxiety
  • Counseling to provide emotional support
  • Nutritional guidance to maintain a healthy diet
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13 Days of Hospitalization Required
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Average Time for Outpatient Care Not Established

Other congenital malformations of spinal cord - Prevention

Prevention of other congenital malformations of the spinal cord involves a combination of pre-pregnancy counseling, genetic testing, and prenatal screening. pre-pregnancy counseling should include information about the risks of the condition, the importance of folic acid supplementation, and the need for regular prenatal care. genetic testing can be used to identify those at risk of having a child with a spinal cord malformation. prenatal screening can help identify those pregnancies at risk of having a baby with a spinal cord malformation, allowing for earlier intervention and improved outcomes.

Specified forms of the disease

(Q06.0) Amyelia
(Q06.1) Hypoplasia and dysplasia of spinal cord
(Q06.2) Diastematomyelia
(Q06.3) Other congenital cauda equina malformations
(Q06.4) Hydromyelia
(Q06.8) Other specified congenital malformations of spinal cord
(Q06.9) Congenital malformation of spinal cord, unspecified