What characterizes autosomal recessive disorders?

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Autosomal recessive disorders are characterized by the necessity of inheriting two recessive alleles for a particular trait or disorder for it to manifest in an individual. This means that both parents must pass on a recessive allele for the disorder to appear in their child. If an individual has only one recessive allele, they are typically carriers but do not exhibit any symptoms of the disorder themselves.

In autosomal recessive conditions, the presence of the two recessive alleles is what leads to the expression of the disorder. For instance, if both parents are carriers (each carrying one recessive allele and one dominant allele), there is a 25% chance that the offspring will inherit two recessive alleles and display the disorder. This genetic scenario helps in understanding the inheritance patterns of many diseases, such as cystic fibrosis and sickle cell anemia.

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