The term Ashkenazi refers to individuals descended from the medieval Jewish communities of the Rhineland in the west of Germany. Many Ashkenazi Jews (AJ) migrated to other parts of Europe, with the majority migrating eastward.
The conditions for which carrier screening is offered are more common in individuals of Ashkenazi Jewish descent than other ethnic groups because of specific mutations that occurred in "founders" of the population. Because Jewish individuals historically married within their own ethnic group, these mutations increased in frequency over generations.
Screening is available for eleven genetic disorders. Carrier frequency is different for each condition — the overall chance of being a carrier for at least one of these diseases is 1 in 4 to 1 in 5 for someone of AJ descent.
Cystic fibrosis (CF) is also common in individuals of Caucasian ancestry. All of these disorders are also found in non-Jewish individuals, but with lower incidence (with the exception of CF).
Clinically Available Screening for Individuals of Ashkenazi Jewish Descent*
Carrier Detection Rate
Tay Sachs disease
Fanconi Anemia group C
Mucolipidosis type IV
Niemann-Pick disease type A
Glycogen Storage 1a
Maple syrup urine disease
* Disease incidence, carrier frequency and detection rates among individuals who are not of Ashkenazi Jewish descent are available by contacting a genetic counselor at the UCSF Prenatal Diagnostic Center.
Based on recommendations from the American College of Medical Genetics, the American College of Obstetrics and Gynecology, and other groups, you should consider carrier screening if you, your partner, or both are of AJ descent.
Carrier screening is typically performed stepwise by screening the individual with AJ ancestry. It is recommended to start with testing of the Ashkenazi Jewish partner and to test the non-Jewish member of the couple only if the Jewish partner is a carrier of any of the diseases. Carrier screening is less sensitive and less informative in non-Jewish individuals.
When both partners are AJ, carrier screening can be done on either partner. Carrier screening can be done simultaneously for both parents, if time is a constraint.
The ideal time to undergo carrier screening is before pregnancy, but carrier screening can be done during pregnancy. If you are already pregnant, we recommend having carrier screening as early in the pregnancy as possible so the results are available to you for further decision making.
All of these conditions are inherited in an autosomal recessive manner. Your test could reveal several different results:
If you are interested in pursuing carrier screening for some or all of these conditions, please contact the Prenatal Diagnostic Center for an appointment.
Please note that medical insurance plans vary widely. Plans may cover the cost of screening at different rates. Our office can help you determine your plan's coverage and facilitate an insurance authorization if required.
Reviewed by health care specialists at UCSF Medical Center.
This information is for educational purposes only and is not intended to replace the advice of your doctor or health care provider. We encourage you to discuss with your doctor any questions or concerns you may have.
Prenatal Diagnostic Center
350 Parnassus Ave., Suite 810
San Francisco, CA 94117
Phone: (415) 476-4080
Fax: (415) 353-4077