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A carrier is a person who can pass an inherited (genetic) disease on to his or her children but who does not have the disease. The person can also pass on carrier status.
Some diseases are caused by defects in a person's chromosomes or genes. Each person inherits 23 chromosomes from each parent and so has 23 pairs of chromosomes. One or both of the chromosomes in a pair may be damaged or defective in a way that causes an inherited (genetic) disease.
The chromosomes are made up of genes. A gene is a portion of DNA that controls or helps control one trait, such as eye color or hair texture. A change in a gene can cause a genetic disease. In some cases the same gene on both chromosomes in a pair must be defective for the person to have the disease. This is known as an autosomal recessive disease. If only one of the genes in the pair is affected, the person is a carrier.
Some genetic disorders are caused by defects in the X or Y chromosome. These chromosomes determine a person's sex.
Current as of:
October 13, 2016
Adam Husney, MD - Family Medicine & Kathleen Romito, MD - Family Medicine & Martin J. Gabica, MD - Family Medicine & Siobhan M. Dolan, MD, MPH - Reproductive Genetics
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