![]() ![]() Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, or a smaller Securities Act registration statement number of the earlier effective registration statement for the same offering. If this Form is a post-effective amendment filed pursuant to Rule 462(d) under the Securities Act, check the following box and list the If this Form is a post-effective amendment filed pursuant to RuleĤ62(c) under the Securities Act, check the following box and list the Securities Act registration statement number of the earlier effective registration statement for the same offering. ¨įiled to register additional securities for an offering pursuant to Rule 462(b) under the Securities Act, check the following box and list the Securities Act registration statement number of the earlier effective registration statement for the same Under the Securities Act of 1933, check the following box. If any of the securities being registered on this Form are to be offered on a delayed or continuous basis pursuant to Rule 415 (Name, address, including zip code, and telephone number, including area code, of agent for service)Īpproximate date of commencement of proposed sale to the public: As soon as practicable after the effective date of this Registration Including zip code, and telephone number, including area code, of registrants principal executive offices) (Exact name of registrant as specified in its charter) Securities and Exchange Commission on March 24, 2014. Both of these procedures carry around a one in 100 risk of causing a miscarriage.As filed with the U.S. This reduction in the false positive rate reduces the number of women being offered invasive testing, using chorionic villus sampling (CVS) or amniocentesis. The Harmony test has a false positive rate of 0.1%. What are the other screening tests available and why is the Harmony test better?Ĭurrent screening tests(Nuchal Translucency scan)have a false positive rate (that is, the results suggest a problem when the baby is in fact healthy) of around 4%. For this reason, a procedure such as an amniocentesis or chorionic villus sampling (CVS) may be recommended following a high probability Harmony result. ![]() What if I have a high probability test result?Ī high probability result does not mean your baby definitely has a chromosomal abnormality although it is highly likely. If the test result shows a high probability result, then the probability that your baby has a chromosomal abnormality is greater than 99%. If the test result shows a low probability result for a chromosomal abnormality, then your baby will have a probability of less than 1 in 10,000. ![]() The Harmony test is now one of the most accurate and non-invasive tests available to predict the chance of your baby having a chromosomal abnormality. In the event of a high probability result, we will provide you with a referral letter to a Fetal Medicine Unit in an EPAU in order to discuss your next steps. If it reports low probability, no further follow up required. The results will come back as 0.01% probability which is your low chance result or 99.9% which is your increased probability result. Once you receive the email/results you can always contact us if there is anything you need to discuss. You will be contacted by a member of our team who will explain the test results to you. Your results will be reported to you within 8 working days of your appointment. You may require an ultrasound scan to confirm gestational age, if you have not already had an early pregnancy scan completed. You will then be asked to complete a consent form. You can have the Harmony Test performed from 10 weeks gestation on How Is The Test Performed & How Long Will It Take To Get The Results?īefore the blood test is taken, the sonographer will discuss the test with you to answer any questions you may have. When can I have the Harmony Test performed 80% of babies with Patau’s syndrome (Trisomy 13).98% of babies with Edwards syndrome (Trisomy 18).99% of babies with Down’s syndrome (Trisomy 21).cfDNA is the result of the natural breakdown of fetal cells and can be found in the mother’s blood. It is a simple blood test taken from the mother which is then analysed for cell-free DNA (cfDNA) from the fetus. The harmony test is a non-invasive prenatal screening test (NIPT) which can be performed from 10 weeks gestation*. Go to form What is the Harmony Test (NIPT) ? ![]()
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