(Q39.8) Other congenital malformations of oesophagus

More details coming soon

Icon
132 175 in individuals diagnosis other congenital malformations of oesophagus confirmed
Icon
2 965 deaths with diagnosis other congenital malformations of oesophagus
Icon
2% mortality rate associated with the disease other congenital malformations of oesophagus

Diagnosis other congenital malformations of oesophagus is diagnosed Men are 7.95% more likely than Women

71 344

Men receive the diagnosis other congenital malformations of oesophagus

1 856 (2.6 %)

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
60 831

Women receive the diagnosis other congenital malformations of oesophagus

1 109 (1.8 %)

Died from this diagnosis.

Risk Group for the Disease other congenital malformations of oesophagus - Men and Women aged 0

Icon
In Men diagnosis is most often set at age 0-39, 45-94
Icon
Less common in men the disease occurs at Age 40-44, 95+Less common in women the disease occurs at Age 30-34, 90-95+
Icon
In Women diagnosis is most often set at age 0-29, 35-89

Disease Features other congenital malformations of oesophagus

Icon
Absence or low individual and public risk
Icon

Other congenital malformations of oesophagus - what does this mean

Other congenital malformations of the oesophagus occur when the oesophagus does not develop normally in the womb, leading to structural defects such as stenosis, atresia, or duplication. these malformations can cause difficulty swallowing, choking, and/or vomiting.

What happens during the disease - other congenital malformations of oesophagus

Other congenital malformations of the oesophagus are caused by genetic or environmental factors, such as chromosomal abnormalities or exposure to certain toxins in the mother's womb during pregnancy. these abnormalities can lead to structural defects in the oesophagus, including narrowing or complete obstruction of the oesophagus, which can cause difficulty in swallowing, vomiting, and poor nutrition. in some cases, the oesophagus may be absent or connected to another organ, such as the trachea or stomach.

Clinical Pattern

More details coming soon

How does a doctor diagnose

  • Physical examination
  • X-rays
  • Ultrasound
  • CT scan
  • MRI scan
  • Endoscopy
  • Biopsy

Treatment and Medical Assistance

Main goal of the treatment: To reduce the symptoms and improve the quality of life for individuals with Other Congenital Malformations of the Oesophagus.
  • Prescribe medications to reduce symptoms such as pain and difficulty swallowing.
  • Refer to a specialist for surgical intervention.
  • Provide nutritional counseling to help with dietary needs.
  • Provide education on the disease and lifestyle modifications to improve quality of life.
  • Monitor for signs of complications such as infection.
  • Regular follow-up visits to monitor the patient’s progress.
Icon
27 Days of Hospitalization Required
Icon
Average Time for Outpatient Care Not Established

Other congenital malformations of oesophagus - Prevention

Prevention of other congenital malformations of the oesophagus can be achieved through pre-pregnancy counselling, genetic testing, and taking folic acid supplements during pregnancy. additionally, pregnant women should be monitored for any signs of oesophageal malformations and receive regular ultrasounds to detect any abnormalities.

Specified forms of the disease

(G32.0*) Subacute combined degeneration of spinal cord in diseases classified elsewhere
(G32.8*) Other specified degenerative disorders of nervous system in diseases classified elsewhere