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Skip Navigation LinksHome Page    >    The various genetic diseases    >    Creutzfeldt Jakob syndrome
 
 
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Creutzfeldt Jakob syndrome


Types and clinical signs

Creutzfeldt Jakob syndrome is a degenerative disease of the brain. The cause is not always genetic, and some people have been infected by injection of brain products (growth hormone that used to be extracted from brains) into their blood or by ingestion of uncooked brain products, which used to be a custom in some parts of Africa.

Inheritance pattern

Autosomal dominant.

Penetrance

Almost always complete, but age dependent. The mean age at which the mental degeneration starts is 60 years. By the age of 80, 96% of the carriers of the mutation are affected.

Associated features that can be demonstrated in tests performed during pregnancy

There are usually no defects. This condition cannot be diagnosed in pregnancy in a family that does not already have affected children.

What is the risk of recurrence in a subsequent pregnancy?

A parent carrying the mutation has a 50% chance in every pregnancy of transmitting it to his or her offspring.

Molecular genetic information

The gene for the disease

PrP gene.

Location

???

Genetic testing

Diagnostic testing

The mutation E200K is tested for in families with affected individuals. See information sheet: Testing the disease-causing gene for mutations that are common in a specific ethnic group - autosomal dominant diseases.

Carrier testing

Carrier testing is in fact the same as diagnostic testing - see above.

Fetal testing

See in section on diagnostic testing.
 
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