Acute myocardial infarction is a medical condition that falls inside the WHO's range ICD-10 code I21.
<h3>What is acute myocardial infarction?</h3>
- A condition in which the myocardium exhibits severe necrosis as a result of a disruption in the blood supply.
- Blood coagulation in one or more coronary arteries.
- A blood clot (thrombus) is a common factor in myocardial infarction.
- Complete obstruction of one of the coronary arteries, typically caused by coronary atherosclerosis.
- In the United States, approximately a million people suffer a heart attack annually.
- Most of them pass away. Because they don't seek care right away, a lot of people suffer permanent heart disease or pass away.
- These symptoms include shortness of breath, chest discomfort (such as pressure, squeezing, or pain), and discomfort in the upper body (such as in the arms, shoulders, neck, and back).
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Answer:
Harmful mutations may cause genetic disorders or cancer. A genetic disorder is a disease caused by a mutation in one or a few genes. A human example is cystic fibrosis. A mutation in a single gene causes the body to produce thick, sticky mucus that clogs the lungs and blocks ducts in digestive organs.
Mutations arise spontaneously at low frequency owing to the chemical instability of purine and pyrimidine bases and to errors during DNA replication. Natural exposure of an organism to certain environmental factors, such as ultraviolet light and chemical carcinogens (e.g., aflatoxin B1), also can cause mutations.
only a small percentage of mutations cause genetic disorders—most have no impact on health or development. For example, some mutations alter a gene's DNA sequence but do not change the function of the protein made by the gene.
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