Autosomal Recessive Disease
Each person inherits 23 chromosomes from each parent and so has 23 pairs of chromosomes. Each chromosome contains genes. One or both of the chromosomes in a pair may contain a changed (mutated) gene that could cause a genetic disease. In an autosomal recessive disease, both chromosomes in a pair must have a changed gene for the person to have the disease. If only one chromosome has a changed gene, the person is a carrier and does not have symptoms.
If both parents carry the gene change, there is a:
If only one parent carries the gene change, there is a 50% chance in each pregnancy that the child will:
If neither parent carries the gene change, the child will not have this type of disease.
See a diagram of the chances of passing on an autosomal recessive disease.
eMedicineHealth Medical Reference from Healthwise
To learn more visit Healthwise.org
© 1995-2014 Healthwise, Incorporated. Healthwise, Healthwise for every health decision, and the Healthwise logo are trademarks of Healthwise, Incorporated.
- Early Care for Your Premature Baby
- What to Eat When You Have Cancer
- When to Take More Pain Medication