Autosomal recessive inheritance
Genes are the blueprints for making the proteins our bodies need to develop and work properly. Most genes come in pairs, one of which is inherited from the mother and the other from the father. A mutation is a change in a gene that prevents it from working properly. Mutations in genes are inherited from our biological parents in specific ways. One of the basic patterns of inheritance of our genes is called autosomal recessive inheritance.
What is autosomal recessive inheritance?
Autosomal recessive inheritance means that the gene carrying the mutation is located on one of the autosomes (chromosome pairs 1 through 22) — meaning that males and females are equally affected. “Recessive” means that both copies of the gene must have a mutation in order for a person to have the trait. One copy of the mutation is inherited from the mother, and one from the father. A person who has only one recessive gene mutation is said to be a “carrier” for the trait or disease, but he or she does not have any health problems from carrying this one mutation. Most people do not know they carry a recessive gene mutation for a disease until they have a child with the disease. Once parents have had a child with a recessive disease, there is a one out of four, or 25 percent chance, with each subsequent pregnancy for another child to be born with the same disorder — meaning that there is a three out of four, or 75 percent chance, for another child not to have the disease.
The birth of a child with a recessive condition is often a total surprise to a family, since in most cases there is no previous family history of the condition. Many autosomal recessive conditions occur this way. Almost all people carry some recessive genes that cause genetic diseases or conditions. It is only when a person has a child with a partner that carries the same recessive gene mutation, that there is a chance of having a child with a recessive disorder. Mutations in certain genes have occurred over time in different parts of the world. Virtually anyone can carry a mutation in any one of the recessive genes; however, there may be certain ethnic groups more likely to carry certain recessive gene mutations, because of where the mutation originated.
Some examples of cancer susceptibility conditions with autosomal recessive inheritance include xeroderma pigmentosum, fanconi anemia and ataxia telangiectsasia.