Sickle-cell anemia
A person who has inherited an autosomal recessive disorder will have two copies of the mutated gene, one from each parent. This results in the individual expressing the disorder. Symptoms can vary depending on the specific disorder.
Some examples of metabolic disorders inherited in an autosomal recessive manner include phenylketonuria (PKU), cystic fibrosis, and Tay-Sachs disease. In autosomal recessive inheritance, two copies of the abnormal gene are needed to manifest the disorder.
Bassen-Kornzweig syndrome is inherited as an autosomal recessive disorder, which means that parents of affected individuals are themselves unaffected carriers, and that they have a 25% risk of having an affected child.
the disorder is usually either autosomal recessive or autosomal dominant. they are passed down from the parents to the next generation. autosomal reccessive diseases only are when one parent gives one reccessive allele and the other parent gives the other reccessive allele. A dominant autosomal disorder can be inherited with one or two of the alleles.
You did not list a "these" to chose from.
PKU is described as an inherited, autosomal recessive disorder.
Yes, Canavan disease is an inherited genetic disorder caused by mutations in the ASPA gene. It is inherited in an autosomal recessive pattern, meaning that an individual must inherit two copies of the mutated gene (one from each parent) to develop the disease.
It is autosomal recessive and it is not a disorder! Cystic Fibrosis is a disease.
C. Sickle-cell anemia
Marfan's Syndrome is inherited in an autosomal dominant pattern. This disease is a disorder that affects the connective tissue in many parts of the body.
hey I'm not positive but I believe that Cystic Fibrosis is autosomal. My reasonning for this is that there seems to be an equal number of females that have cystic fibrosis as there are males. I AM NOT POSITIVE.
Tay Sachs Disease