Home Contact Us Site Map
Search for:
Mercy Babies Classes News
Health Info Find a Job Find a Physician
Mercy Health Center
Oklahoma City
Quick Facts
Our Ministry
Foundation
Medical Services
Patient & Guest Services
Mercy Quality
Mercy Memorial
Health Center

Ardmore
Mercy Health
Network Clinics

Oklahoma City
Mercy NeuroScience
Institute

Oklahoma City
Oklahoma
Heart Hospital

Oklahoma City
 
Home > Mercy Health Center > Medical Services > Cancer Services > Educational Resources > Cancer Library 

Link to Cancer OverviewLink to Cancer DiagnosisLink to Cancer TreatmentLink to Cancer TypesLink to Pediatric CancersLink to Genetics and CancerLink to Nutrition and CancerLink to Alternative TherapyLink to Pain ManagementLink to Clinical Trial Overview

Autosomal Recessive Inheritance

Genes are the blueprints for making the substances, called 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?

Genetic illustration demonstrating autosomal recessive inheritance
Click Image to Enlarge

Autosomal recessive inheritance means that the gene carrying the mutation is located on one of the autosomes (chromosome pairs 1 through 22). This means 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/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. This means that there is a three out of four, or 75 percent chance, for another child to not 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. It is estimated that all people carry about 20 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.

Click here to view the
Online Resources of Cancer Center

Center Home

A member of the
Sisters of Mercy Health System