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Skip Navigation LinksHome Page    >    Tests during the pregnancy    >    Indirect testing for genetic markers in a family that has one or several patients - when there are a number of genes that can each cause the disease - the gene, or most of the genes not having been located / identified / mapped - X-linked diseases
 
 
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Indirect testing for genetic markers in a family that has one or several patients - when there are a number of genes that can each cause the disease - the gene, or most of the genes not having been located / identified / mapped - X-linked diseases


This is not a direct test, but a comparative one, which is called linkage analysis. The alleles (an allele is one member of the pair of genes at a given disease locus) that have been transmitted by the parents to the affected child are compared in order to establish which of the mother-s two X chromosomes the affected child has inherited. If the mother is a carrier of an X-linked disease, she has a normal gene on one of her X chromosomes and an abnormal gene on the other. Such a woman has a 50% chance in every pregnancy of transmitting the abnormal gene to her offspring. This means that 50% of her sons will be affected and 50% healthy, and 50% of her daughters will be carriers and 50% will not.

In genetic linkage studies, alleles of each of the genes being tested are compared between the patients and the healthy family members. The allele that is present only in the patients but in none of the healthy family members - i.e. the -shared allele- of these patients - is the one in which the mutation responsible for the disease is located. If the -shared allele- is found, it will be possible to test other family members without identifying the mutation itself, and prenatal testing by amniocentesis or chorionic villus sampling can be carried out. This is done by looking for the -shared allele- in the DNA of the affected individuals in the family. It is also possible to establish which women in the family are carriers.

Because the location of the disease-causing genes, or most of the genes, has yet to be identified, the test cannot be completed - it takes a long time and will not be completely reliable.

If there are a number of genes that can cause the disease, the problem is even more severe.

However, in very large families with a large number of patients (at least 7), an attempt can be made.

This can be done by performing a comparative test for each of the regions in the genome (or candidate areas).

Only in the locus containing the gene responsible for the disease will there be complete correlation between the genotype and the phenotype - in other words, the -shared allele- will be found in all the patients, but in none of the healthy relatives. In the other loci, complete genotype-phenotype correlation will not be found.

The test requires comparison of a number of affected and healthy members of the same family. The test is only reliable if DNA from several affected individuals in the family is already available, or if it can be obtained from a blood (or other) sample. The cooperation of the family members is required - they must be examined by a physician in order to ascertain whether they have signs of the disease, and must agree to give a blood sample. The more candidate genes there are the more complex and difficult it is to perform the test, as a new gene must in fact be identified.
 
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