Because as they are homozygous recessive they are only lethal when a person inherits an allele from both parents, meaning that each parent must be heterozygous carriers of the gene, and even then it's only a 1 in 4 chance that the offspring will be homozygous recessive and therefore it's unlikely they will die. And if they do not die then the will survive to likely pass on the gene.
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.
If they are expressing the trait, 100%, as their genotypes would be, rr X rr If they both carry the trait and it is dominated, Rr X Rr, then the probability would be, 25% of their child expressing the trait.
None. =]
Althought the diabetes skipped many generations in my family, it was apparently a recessive trait because the newborn was diagnosed with the disease.
Sickle cell disease is an autosomal recessive disorder, meaning that it is caused by a mutation in one of the autosomal chromosomes (chromosomes that are not sex chromosomes). In the case of sickle cell disease, the mutation occurs in the gene encoding the beta-globin subunit of hemoglobin on chromosome 11.
Wilson's disease is recessive
recessive
Recessive
a woman who is heterozygous for the gene
Yes, cystic fibrosis is an autosomal recessive disease.
Cystic fibrosis is an autosomal recessive genetic disease. A+ neuromuscular disease
The disease is recessive, requiring both parents to carry the allele for the disease to be found in the offspring. If one parent has it, the offspring can also be a carrier, but it will be recessive, and the offspring will have normal RBC (red blood cells)
its ressesive
It is Dominant.
recessive
Cystic fibrosis is an autosomal recessive genetic disease.
A recessive disease is not able to be passed on if both parents are carriers of the gene but do not express the disease themselves. In this case, the offspring would only inherit the disease if they receive two copies of the recessive gene, one from each parent. If the child inherits only one recessive gene and one dominant gene, they will be a carrier but will not exhibit the disease. Thus, the disease can only be passed on if both parents contribute the recessive allele.