Men have 1 X chromosomes and Women have 2. This means, that men are more affected by the x linked recessive disorder as they only have one chance to get a non mutant allele. See the wikipedia extert below for more info.
"In humans, generally "men are affected and women are carriers" for two reasons. The first is the simple statistical fact that if the X-chromosomes is a population that carry a particular X-linked mutation at a frequency of 'f' (for example, 1%) then that will be the frequency that men are likely to express the mutation (since they have only one X), while women will express it at a frequency of f2 (for example 1% * 1% = 0.01%) since they have two X's and hence two chances to get the normal allele. Thus, X-linked mutations tend to be rare in women."
Males, of course. Only males have Y chromosomes. Females are XX in sex chromosome number.
It depends what the trait is.
Autism is not traditionally x-linked. If it were x-linked dominant, all females of an affected father would have it (since they always get one x from their fathers). If it were x linked recessive, then it would skip a generation and NO male sons of an affected father would have Autism. There is evidence that there is a relation to sex, given the increased ratio of affected boys to girls, but it's a complicated mix of genetic and nongenetic causes (i.e. imprinting of genes, comorbid diagnoses).
Males are more likely to receive a sex-linked genetic trait because they have only one X chromosome. A certain trait on a woman's X may be covered up by another trait on her other X, men only have one X so they are stuck with whatever trait appears on it.
color blindness is one
An X-linked recessive trait is coded for by a gene on the X-chromosome and is not dominant (is canceled out by the presence of a different allele). Example of X-linked recessive traits are; Haemophilia A & B and Duchenne muscular dystrophy.
For a recessive sex-linked trait to manifest in women it would have to be in double dose (XaXa) while for men in single dose (XaY). Women carriers would have one of each but would not be affected (XAXa). Knowing this it's quite easy to spot pedigrees where this kind of inheritance occures.Heterozygote mothers (gene carrier) can have sons that are affected (50% chance);Affected mothers have only affected sons (100%);No first generation daughter of an heterozygote mother will be affected but there is a 50% chance that she is a carrier;Affected fathers with normal mothers will have zero sons that are affected but all their daughters will be carriers;
There are 2 X-linked recessive inheritance where Only Male or Men are the only people who inherits these kind of trait.
recessive
Some are dominant ... some of the most noteworthy negative ones: color blindness, hemophilia are recessive.
Because they olny have one X chromosome.
Because they olny have one X chromosome.
Autosomal dominant, Autosomal recessive, X-linked recessive and X-linked dominant
Yes, it is X linked recessive.
Males
Rare X-linked recessive
Sex-linked and Recessive
get a test
Muscular dystrophy is a sex-linked recessive disorder.