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There are several disorders that are caused by abnormal sex-linked traits. In addition to hemophilia, other x-linked recessive disorders include color blindness, duchenne muscular dystrophy, and fragile-x syndrome. A female with turners syndrome has only one x chromosome and is sterile. X-iinked recessive diseases advertisements hemophilia a and b, color blindness, duchenne muscular dystrophy. Sex-linked disorders are those that are inherited from genes located on the sex chromosomes, x or y in humans. Some examples of x-linked disorders are duchenne muscular dystrophy, hemophilia and. Human genetic disease - human genetic disease - sex-linked inheritance in humans, there are hundreds of genes located on the x chromosome that have no counterpart on the y chromosome. The traits governed by these genes thus show sex-linked inheritance. This type of inheritance has certain unique characteristics, which include the following (1) there is no male-to-male (father-to-son.). Describe and diagram the inheritance of an autosomal dominant disorder 3. Describe and diagram the inheritance of a sex-linked disorder 4. Distinguish between the 4 major types of genetic screening available. All genetic conditions are called disorders and those that inherit them are called sufferers. Most genetic disorders, like cystic fibrosis, require two recessive. Sex-linked disorders, also known as x-linked diseases, refer to defects in the x chromosome that are inherited and cause certain diseases. According to medlineplus, x-linked diseases typically are most severe in males as they only have one x chromosome while females have two x chromosomes 2. X-linked disorders result from mutated genes on the x chromosome. , they are hemizygous), will fully express an x-linked disorder. On the other hand, females, who have two x chromosomes, will be carriers of the defect in the majority of cases, and so they are usually asymptomatic. X-linked recessive inheritance is a mode of inheritance in which a mutation in a gene on the x chromosome causes the phenotype to be always expressed in males (who are necessarily homozygous for the gene mutation because they have one x and one y chromosome) and in females who are homozygous for the gene mutation, see zygosity.

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