Autosomal recessive conditions are genetic diseases that are passed to a child through both parents' chromosomes. Autosomal recessive diseases include Tay-Sachs disease, cystic fibrosis, sickle cell disease, autosomal recessive polycystic kidney disease (ARPKD), and phenylketonuria (PKU).
Each person inherits 23 chromosomes from each parent and so has 23 pairs of chromosomes. Each chromosome contains genes. One or both of the genes in a pair can carry a mutation and fail to function properly. In an autosomal recessive condition, both chromosomes in a pair must have a mutation for the person to have the disease. If only one gene carries a mutation, the person is a carrier of the condition but does not have any symptoms.
Carrier test information for autosomal recessive conditions
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One parent is a carrier
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Both parents are carriers
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If only one parent carries a mutation, there is:
- A 50% chance in each pregnancy that their child will receive the mutation and be a carrier.
- A 50% chance in each pregnancy that their child will not receive the mutation and will not be a carrier or have the condition.
- Almost no chance that their child will have the condition.
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If both parents carry a mutation, there is:
- A 25% chance in each pregnancy that their child will inherit the mutation from each parent (two genes) and have the condition.
- A 50% chance in each pregnancy that their child will receive one mutated gene and be a carrier.
- A 25% chance in each pregnancy that their child will not receive the mutated gene and will not be a carrier or have the condition.
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Current as of: July 31, 2024
Author: Ignite Healthwise, LLC Staff
Clinical Review Board
All Healthwise education is reviewed by a team that includes physicians, nurses, advanced practitioners, registered dieticians, and other healthcare professionals.
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