(Q23) Congenital malformations of aortic and mitral valves

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454 048 in individuals diagnosis congenital malformations of aortic and mitral valves confirmed
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13 887 deaths with diagnosis congenital malformations of aortic and mitral valves
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3% mortality rate associated with the disease congenital malformations of aortic and mitral valves

Diagnosis congenital malformations of aortic and mitral valves is diagnosed Men are 34.83% more likely than Women

306 107

Men receive the diagnosis congenital malformations of aortic and mitral valves

8 957 (2.9 %)

Died from this diagnosis.

100
95
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75
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55
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147 941

Women receive the diagnosis congenital malformations of aortic and mitral valves

4 930 (3.3 %)

Died from this diagnosis.

Risk Group for the Disease congenital malformations of aortic and mitral valves - Men and Women aged 0

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In Men diagnosis is most often set at age 0-89
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Less common in men the disease occurs at Age 90-95+Less common in women the disease occurs at Age 95+
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In Women diagnosis is most often set at age 0-94

Disease Features congenital malformations of aortic and mitral valves

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Absence or low individual and public risk
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Congenital malformations of aortic and mitral valves - what does this mean

Congenital malformations of aortic and mitral valves are caused by abnormal development of the valves during fetal development. these malformations can lead to an obstruction of blood flow through the heart, leading to difficulty in pumping blood and other symptoms associated with heart valve problems.

What happens during the disease - congenital malformations of aortic and mitral valves

Congenital malformations of aortic and mitral valves are caused by abnormal development of the endocardial cushion tissue during fetal development. this results in improper formation of the heart valves, leading to an increase in the pressure in the left side of the heart and a decrease in the pressure in the right side of the heart, resulting in a decrease in the efficiency of the heart to pump blood. this can lead to a variety of symptoms, including heart failure, arrhythmias, and stroke.

Clinical Pattern

More details coming soon

How does a doctor diagnose

  • Physical examination
  • Echocardiography
  • Cardiac catheterization
  • Cardiac computed tomography (CT) scan
  • Cardiac magnetic resonance imaging (MRI)
  • Electrocardiogram (ECG)
  • Chest X-ray
  • Transesophageal echocardiogram (TEE)

Treatment and Medical Assistance

Main goal of the treatment: To improve the patient's symptoms and quality of life.
  • Monitoring of the patient's condition.
  • Regular imaging scans to track the progression of the disease.
  • Medication therapy to reduce symptoms.
  • Surgery to repair the affected valves.
  • Follow-up care to assess the patient's progress.
  • Lifestyle changes to reduce the risk of complications.
  • Counseling to help the patient cope with the disease.
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18 Days of Hospitalization Required
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Average Time for Outpatient Care Not Established

Congenital malformations of aortic and mitral valves - Prevention

The best way to prevent congenital malformations of aortic and mitral valves is through prenatal care. this includes regular check-ups during pregnancy, as well as genetic counseling to assess the risk of the condition. additionally, lifestyle changes such as a healthy diet, regular exercise, and avoiding smoking can help reduce the risk of these malformations.

Specified forms of the disease

(Q23.0) Congenital stenosis of aortic valve
(Q23.1) Congenital insufficiency of aortic valve
(Q23.2) Congenital mitral stenosis
(Q23.3) Congenital mitral insufficiency
(Q23.4) Hypoplastic left heart syndrome
(Q23.8) Other congenital malformations of aortic and mitral valves
(Q23.9) Congenital malformation of aortic and mitral valves, unspecified