C. Sickle-cell anemia
Phenylketonuria is an autosomal recessive genetic disorder. The enzyme phenylalanine hydroxylase is necessary to metabolize phenylalanie, but when this enzyme doesnt work, phenylaline accumulates and is detected in the urine. The disease is detected during pregnancy, and if treated right away the newborn can develop normally. However, if left untreated, the brain will not develop properly.
Huntington's disease is inherited in an autosomal dominant pattern, meaning that only one copy of the mutated gene is needed to develop the disorder. It is not linked to sex chromosomes.
Wilson's disease is an autosomal recessive disorder, meaning that both copies of the gene associated with the disease must be mutated for the individual to develop the condition. It is not a sex-linked disorder, as it does not depend on the individual's sex for inheritance.
Apert syndrome is typically caused by a sporadic mutation in the FGFR2 gene and is not inherited in a simple dominant or recessive manner. It is considered an autosomal dominant condition, with most cases arising from new mutations.
yes it is, only 1 mutation to the lmna gene is sufficent for someone to express traits regarding progeria
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.
Sickle-cell anemia
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.
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.
C. Sickle-cell anemia