Why should I choose Panorama™?
Panorama™ is a test that looks for disorders of the genome in your unborn baby. These disorders can be detected very early in the pregnancy, as early as the 9th week of pregnancy, by means of a blood sample from you as a mother. These defects of the genetic material include, for example, Trisomy 21 (also called Down syndrome), Trisomy 18 (Edwards syndrome), or Trisomy 13 (Patau syndrome). In addition, Panorama™ also detects other defects, such as microdeletions. If these defects are present, the test finds chromosomes that are not complete. This means minute sections of the chromosomes are absent and this can thus lead to mental handicaps and malformations of the organs, as well as the skeleton of the child.
Similar screening tests of this type are also offered. But you should still choose Panorama™.
Panorama ™ offers significant advantages over other tests:
- Because of the unique and highly accurate examination method used on your baby’s genetic material, Panorama™provides more value in its results than other tests.
- Panorama™ is the only test on the market in which the chromosomes are “examined from the inside” – similar to a paternity test. All other test methods count the chromosomes (counting method), which is a significant source of error.
- Over 99% of all cases of Trisomy 21 (Down syndrome), Trisomy 18 (Edwards syndrome), Trisomy 13 (Patau syndrome) and Triploidy are detected by Panorama™.
- Panorama™ is the only test that recognizes chromosomes which are tripled – so-called Triploidy.
- Panorama™ is the only test that recognizes chromosomes of which there is only one, rather than two – so-called Monosomy.
- Can be carried out from the 9th week of pregnancy.
- Results are ready after only 4 – 7 working days.
- Costs can be assumed by the health insurance provider upon request.
- Can be carried out for all pregnant women, of any age and in every stage of pregnancy (after the 9th week of pregnancy).
What can Panorama™ test for?
Panorama™ searches for specific chromosomal abnormalities in the child. At present the following abnormalities can be tested for:
Trisomy 21: This deviation is caused by an additional copy of chromosome 21 and is also referred to as Down syndrome. This is the most common cause of mental disabilities. Trisomy 21 may also cause certain heart defects or diseases of other organs, as well as impairments of hearing or vision.
Trisomy 18: This deviation is caused by an additional copy of chromosome 18 and is also referred to as Edwards syndrome. This syndrome leads to severe mental disability. In addition, it causes severe birth defects that may affect the brain, the heart, and other organs. Children born with Edwards syndrome usually die before the end of their first year.
Trisomy 13: This deviation is caused by an additional copy of chromosome 13 and is also referred to as Patau syndrome. This syndrome leads to severe mental disability. In addition, it causes severe birth defects that may affect the brain, the heart, and other organs. Children born with Patau syndrome usually die before the end of their first year.
Monosomy X (also called Turner syndrome or 45, X): This deviation is caused by a missing copy of the X chromosome and only affects girls. Girls with Monosomy X may have heart defects, hearing impairments, as well as a minor learning disabilities and are usually smaller than average. As adults they are often infertile.
Triploidy: This disorder is caused by an additional copy of all 23 chromosomes (so that a total of 69 chromosomes are present) and is associated with severe birth defects. A pregnancy with a child with Triploidy can be dangerous for the mother because it can lead to excessive bleeding after birth and can be associated with the development of cancer. Women who are expecting a child with Triploidy often suffer a miscarriage, and those children who survive usually die within a few months after birth. It is important that the doctor knows about the Triploidy, even if the mother suffers a miscarriage. Around 12 out of 100 miscarriages are due to Triploidy. Making it one of the main causes of miscarriages. The occurrence of Triploidy is not dependent on the age of the mother.
Klinefelter’s syndrome: This syndrome is caused by an extra copy of the X chromosome, also referred to as 47, XXY, and only affects boys. Boys with Klinefelter’s syndrome can be learning-impaired, are often larger than average, and most men with this syndrome are sterile.
Triple X syndrome: This syndrome is caused by an extra copy of the X chromosome, also referred to as 47, XXX, and only affects girls. Some girls with triple X syndrome have learning disabilities, others have emotional difficulties and most are larger than average.
XYY syndrome: This syndrome is caused by an extra copy of the Y chromosome, also referred to as 47, XYY, and only affects boys. Boys with this syndrome are often larger than average and often have learning and behavioral difficulties.
What can Panorama™ not test for?
Panorama™ cannot be performed if:
- the mother is expecting twins or multiples.
- the mother and father of the baby are blood-related.
- the pregnancy is a result of a single donation or surrogacy.
- The mother previously underwent a bone marrow transplant.
- The microdeletion screening can not be performed on a carrier of microdeletion. Other numerical and structural chromosomal abnormalities than those described, as well as mosaics (mixture of normal and abnormal cells) are not covered by this test.
How secure is Panorama™?
Over 99% of all cases of Trisomy 21 (Down syndrome), Trisomy 18 (Edwards syndrome), Trisomy 13 (Patau syndrome) and Triploidy, as well as approx. 92% of all cases of Monosomy X are detected by Panorama™.
When should I do the test?
If you want to know if your baby is at risk of certain genetic diseases, Panorama™ is the right choice. In some women, the risk of certain disease patterns, such as Down syndrome, is higher, especially with pregnancies over the age of 35, if there is a history of these diseases in the family, or in the case of abnormal ultrasound or blood tests. Microdeletions, which can also be examined with Panorama™, however, occur independent of the age of the mother.
When can I do the test?
You can take the test at any time during your pregnancy. You should however be in the 9th week of pregnancy at least, since the proportion of the baby’s genetic material in the maternal blood is only then available in a sufficient quantity for Panorama ™.
Where can I do the test?
Ask your treating doctor about Panorama™. They will either carry out the test themselves or refer you a prenatal diagnostician or human geneticist who will perform the test.
Where can I buy the test?
You can get the test from your treating doctor or you can order it here via the order form. With the test you have purchased, you can then go to your treating physician and have them perform the test.
How much does the test cost?
The cost of the Panorama ™ test depends on the test package you choose.
We offer four different types of testpanels.
All offered test packages are performed with the unique SN (i) P test technology.
Please note that in addition to Panorama™, the separate costs of the treating doctor will be charged. In exceptional cases, the health insurance provider assumes the cost of the test. However, you and your doctor must separately apply for this cost assumption from your health insurance provider. You can find a template for this application for cost assumption in our download section.
Who pays for the test?
The Panorama™ test is a medical service that is billed according to the doctor’s fee schedule (GOÄ). For medical services, there is the possibility of cost assumption by the statutory or private health insurance provider on request. A partial or complete cost-assumption is at the discretion of the insurance provider. If appropriate, the treating doctor can additionally certify the medical necessity of the examination (a template for a health insurance application for the cost assumption can be found under Downloads).
When and where do I get the test results?
The results will be communicated to the doctor who performed the Panorama ™ test within 7-10 calendar days. Your doctor will then give you the results in a personal interview and clarify any open questions. Further information on the test results can also be found in our patient manual on the test results.
The test is positive, what then?
Panorama™ is a screening test. The result is indicated as a high or low risk for each analyzed syndrome. If a high risk exists, a confirmation of the result using invasive diagnostics is urgently required. Further information on the test results can also be found in our patient manual on the test results.