Sex-linked diseases are inherited through one of the "sex chromosomes" -- the X or Y chromosomes. Autosomally inherited diseases are inherited through the non-sex chromosomes (autosomes), pairs 1 through 22.
Dominant inheritance occurs when an abnormal gene from one parent is able to cause disease even though the matching gene from the other parent is normal. The abnormal gene dominates.
Recessive inheritance occurs when both matching genes must be abnormal to produce disease. If only one gene in the pair is abnormal, the disease does not show up or is mild. Someone who has one abnormal gene (but no symptoms) is called a carrier. A carrier can pass this abnormal gene to his or her children.
The term "sex-linked recessive" usually refers to X-linked recessive.
See also:
Inheritance - sex-linked recessive; Genetics - sex-linked recessive; X-linked recessive
InformationX-linked diseases usually occur in males. Males have only one X chromosome. A single recessive gene on that X chromosome will cause the disease.
The Y chromosome is the other half of the XY gene pair in the male. However, the Y chromosome doesn't contain most of the genes of the X chromosome. It therefore doesn't protect the male. This is seen in diseases such as hemophilia and Duchenne muscular dystrophy.
TYPICAL SCENARIOS
For a given birth, if the mother is a carrier (only one abnormal X chromosome) and the father is normal:
If the father has the disease and the mother is normal:
X-LINKED RECESSIVE DISORDERS IN FEMALES
Females can get an X-linked recessive disorder, but this is very rare. An abnormal gene on the X chromosome from each parent would be required, since a female has two X chromosomes. This could occur in the two scenarios below.
For a given birth, if the mother is a carrier and the father has the disease:
If the mother has the disease and the father has the disease:
The odds of either of these two scenarios are so low that X-linked recessive diseases are sometimes referred to as "male only" diseases. However, this is not technically correct.
Female carriers can have a normal X chromosome that is abnormally inactivated. This is called "skewed X-inactivation." These females may have symptoms similar to those of males.
Sexlinked and recessive.
true
Chocolate is a regional name used by racing pigeon breeders for a recessive opal pigeon. All racing pigeons can live up to about 12-15 years with a rare number of them living to about 20. And even though you didn't specifically ask this, recessive opal is a non-sexlinked (autosomal) recessive.
Color blindness is a recessive trait, meaning that an individual needs to inherit two copies of the gene for color blindness (one from each parent) in order to be color blind. If an individual inherits only one copy of the gene, they are considered a carrier and will not exhibit color blindness.
Anyone can be a carrier of a recessive genetic disorder (as long as it is not associated with the sex chromosomes) no matter what their gender since "carrier" refers to an individual that is heterozygous for the recessive allele and therefore phenotypically normal. Specifically, sexlinked genetic disorders can be "carried" by a heterozygous female but males (having only one X chromosome) cannot. Males will either be free of the defective gene or be affected.
No. Carriers are people that carry the gene for something but exhibit no phenotype for it. Since males have no extra copy to hide a recessive trait, they cannot be carriers for sex linked traits.Answ2. Followers of this question should consult say haemophilia in wikipedia.com.
The trait that is hidden is recessive trait.
Recessive
recessive.
recessive
A recessive phenotype is expressed in an offspring that has a homozygous recessive genotype for that trait.
Recessive alleles are alleles that are masked or overshadowed by dominant alleles. In a heterozygous genotype, the recessive allele does not show its effects. Only in a homozygous recessive genotype does the recessive allele manifest its trait.