Inherited

Inherited refers to the transmission of genetic traits from parents to offspring. These traits are determined by individual genes, which are small segments of DNA carried on chromosomes. Inherited traits can include physical characteristics such as height and eye color, as well as susceptibility to certain health conditions such as heart disease or cancer.

Genetics and Inheritance

The process of inheritance begins when an organism's genes are passed on to its offspring. This occurs through sexual reproduction, where each parent contributes one set of chromosomes to the offspring. The combination of these chromosomes determines the offspring's genetic makeup and, consequently, its traits.

In humans, each cell normally contains 23 pairs of chromosomes, for a total of 46. Twenty-two of these pairs, called autosomes, look the same in both males and females. The 23rd pair, the sex chromosomes, differ between males and females. Females have two copies of the X chromosome, while males have one X and one Y chromosome.

Inherited Diseases

Inherited diseases are health conditions that are passed down from parents to children through genes. These diseases can be caused by a variety of genetic defects, from a single mutated gene to an entire missing or extra chromosome. Some examples of inherited diseases include cystic fibrosis, sickle cell anemia, and Down syndrome.

Genetic Testing

Genetic testing is a type of medical test that identifies changes in chromosomes, genes, or proteins. The results of a genetic test can confirm or rule out a suspected genetic condition or help determine a person's chance of developing or passing on a genetic disorder.

See Also

• Genetics
• Chromosome
• DNA
• Genetic disorder
• Genetic testing

References

This article is a medical stub. You can help WikiMD by expanding it!
Most recent articles Ongoing trials	Wikipedia