(Q23.9) Congenital malformation of aortic and mitral valves, unspecified

More details coming soon

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

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

306 107

Men receive the diagnosis congenital malformation of aortic and mitral valves, unspecified

8 957 (2.9 %)

Died from this diagnosis.

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95
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147 941

Women receive the diagnosis congenital malformation of aortic and mitral valves, unspecified

4 930 (3.3 %)

Died from this diagnosis.

Risk Group for the Disease congenital malformation of aortic and mitral valves, unspecified - 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 malformation of aortic and mitral valves, unspecified

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

Congenital malformation of the aortic and mitral valves is an abnormality that is present at birth and is caused by the valves not forming correctly in the womb. this can lead to inadequate blood flow through the valves, leading to symptoms such as shortness of breath, fatigue, and a rapid or irregular heartbeat.

What happens during the disease - congenital malformation of aortic and mitral valves, unspecified

Congenital malformation of aortic and mitral valves is caused by abnormal development of the heart during gestation. this can result in malformations of the valves, including stenosis, regurgitation, or both, which can lead to impaired blood flow through the heart and decreased cardiac output. these malformations can be caused by genetic mutations, chromosomal abnormalities, or environmental factors.

Clinical Pattern

More details coming soon

How does a doctor diagnose

  • Physical examination
  • Echocardiogram
  • Cardiac catheterization
  • Electrocardiogram (ECG)
  • Chest X-ray
  • MRI scan
  • CT scan
  • Blood tests
  • Ultrasound
Additional measures:
  • Cardiac MRI
  • Cardiac CT

Treatment and Medical Assistance

Main goal of the treatment: To improve the function of the aortic and mitral valves and reduce symptoms associated with the malformation.
  • Medication to reduce symptoms and improve valve function
  • Regular monitoring of cardiac function
  • Lifestyle changes to reduce stress on the heart
  • Surgery to repair or replace the valves
  • Rehabilitation to improve physical and mental health
  • Counseling to address any psychological issues
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18 Days of Hospitalization Required
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Average Time for Outpatient Care Not Established

Congenital malformation of aortic and mitral valves, unspecified - Prevention

The best way to prevent congenital malformation of aortic and mitral valves is to get regular prenatal care. this includes taking folic acid, avoiding smoking and alcohol, and getting regular ultrasounds to check for any abnormalities. additionally, it is important to maintain a healthy lifestyle and diet to ensure the best possible health of the unborn baby.

Specified forms of the disease

(M20.0) Deformity of finger(s)
(M20.1) Hallux valgus (acquired)
(M20.2) Hallux rigidus
(M20.3) Other deformity of hallux (acquired)
(M20.4) Other hammer toe(s) (acquired)
(M20.5) Other deformities of toe(s) (acquired)
(M20.6) Acquired deformity of toe(s), unspecified