At HUMEDIT NIPT, we have everything you need to know, a plan that fits your budget, and a variety of options. Please choose the plan that suits you best.
List of Inspection Plans
The test is performed when there is only one fetus (single fetus) or twins.
Those who wish to have their sex chromosome abnormalities checked in addition to the same tests as in the Minimum Plan.
What you can find out in this plan
Down syndrome, etc. Abnormalities in the number of chromosomes（Chromosomes 13, 18, and 21）※1
Klinefelter’s syndrome, Turner’s syndrome,Abnormal number of sex chromosomes
Gender
In addition to the three chromosomes performed, we will report abnormalities in the number of sex chromosomes.
The HUMEDIT NIPT test for number abnormalities will report not only trisomies but also monosomies.
Those who wish to perform the same inspections as accredited facilities.
Those who wish to reduce inspection costs.
What you can find out about this plan
Down syndrome, Abnormalities in the number of chromosomes（Chromosomes 13, 18, and 21）※1
The test is the same as the test performed at accredited facilities, but the HUMEDIT NIPT test for number abnormalities is reported for monosomies as well as trisomies.
※1：An abnormality in the number of chromosomes occurring in a single chromosome, not including triploids and tetraploids. ※2：Only deletions and duplications of 7 million bases or more. Translocations and inversions are not included.
New Prenatal Testing (NIPT) Over 28,000 completed cases You can take the test
with an easy mind.
There are several NIPT tests available, but which one should I choose… The Minimum Plan seems to be more affordable for the cost of the test, but what do you think?
I know you are probably anxious about the NIPT test because it is not a test that is taken often. The Minimum Plan is an affordable plan that can test for Down Syndrome (Trisomy 21) as well as Trisomy 18 and 13.
Source: HUMEDIT survey
however、minimum planThen, of the HUMEDIT NIPT tests that are positive48%It can only be detected in Trisomy of all chromosomes is more likely to occur, especially in pregnant women over 35 years of age, soover35 Planis recommended.
Full Set PlanwellAll chromosomes 1-22not just … (but also ..) over35 Planandlight planThe content will showwhole autosomal whole region partial deletion/duplication diseasesthat cannot be detected by.
This plan is perfect for people who “want to take this opportunity to check for detailed anomalie”.
Source: HUMEDIT survey
I see that you can now take the new stand-alone chromosome test.
If it were a single chromosome, it would beI need to know only chromosome 21 (Down syndrome).You can also test for people who have Also, you can choose to have a specific chromosome abnormality in a relative and want to test only for that.
You can choose tests that are not available elsewhere, while at the same timeAt HUMEDIT, you can receive a safe and reliable examination at a reasonable cost.
New Prenatal Testing (NIPT) Over 28,000 completed cases You can take the test
with an easy mind.
Distribution of Positive Cases of HUMEDIT NIPT (June 2020~)
Source: HUMEDIT survey
The chart above shows the distribution of positive cases since June 2020. About a quarter of the positive cases tested at Hiro Clinic NIPT fall into the Autosomal Stand-alone Testing Plan(Chromosomes 1 to 22) that tests for Trisomy 21.
The Minimum Plan which tests for trisomy 21, 18, and 13, which are included in the NIPT Consortium testing, accounts for 48% of the total number of positive results. In addition to trisomy 21, 18, and 13, which can be tested in the over35 Plan and Full Set Plan, Autosomal trisomy/monosomy other than chromosomes 21,18 &13 accounts for 21% of the total number of positives. In particular, trisomy on all chromosomes is more likely to be detected in pregnant women over 35 years of age, and we recommend that these tests be performed in pregnant women over 35 years of age.
The All autosomal partial deletions and duplications, which is included in the Full Set Plan, account for 18% of the total number of positive cases, about the same as the number of positive cases for Trisomy 18.
The detection of All autosomal partial deletions and duplications is likely to involve more than 7 million base pairs, which includes about 140,000 base pairs of exon regions, which are likely to be moderately to severely disabling. In some cases, even a single base change in an exon region can cause disease.
It is important to carefully consider the cost and coverage of the test and choose a test plan that you are satisfied with.
