Confirm pregnancy dating
Bring your antenatal record and any dating scan. The doctor will confirm your pregnancy stage and suitability from 10 weeks onward.
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NICC / NIPT · PRENATAL CHROMOSOME SCREENING
A new chapter.
Space for your questions.
Pregnancy brings hopes, plans and questions. Take time to understand your screening options, with a doctor to guide the conversation.
Non-invasive prenatal chromosome screening from 10 weeks of pregnancy onward, with an ultrasound and two doctor consultations included.
YOUR NICC / NIPT PACKAGE
RM1,200
Nett · No hidden charges for the listed package
- Prenatal chromosome screening
- 1 FREE ultrasound scan with image
- 2 doctor consultations · Fetal sex information
The clinic confirms suitability, appointment timing and the expected report date.
NIPT is screening, not a diagnosis. Your doctor will explain the scope and possible next steps before you decide.
From 10 weeksDoctor confirms eligibility
2 consultations includedNo extra consultation charges
7 working daysExpected report turnaround
INFORMATION, WITH CARE
Understand your options, one step at a time.
Choosing prenatal screening is a personal decision. MyGP’s NICC / NIPT Prenatal Chromosome Screening Package offers expectant mothers information about the chance of selected chromosomal conditions, with doctor consultations to help explain the test and the results.
Available from 10 weeks of pregnancy onward, the RM1,200 nett package includes screening for the listed trisomies, sex chromosome conditions and chromosome-number differences across the 23 chromosome pairs. It also includes one free ultrasound scan with an image, two doctor consultations at no extra charge and fetal sex information. The expected report time is seven working days.
NIPT uses a blood sample from the mother. It is a screening test, so it cannot confirm a diagnosis or rule out every genetic or developmental condition. Your doctor will discuss suitability, the limits of the panel and what different results may mean, helping you make an informed choice alongside your usual antenatal care.
WHAT’S INCLUDED
Your screening, clearly explained.
Explore the chromosome screening and care included in your RM1,200 nett package.
01Trisomy screeningThe six listed trisomy conditions.
Common trisomies
- Down syndrome — Trisomy 21
- Edwards syndrome — Trisomy 18
- Patau syndrome — Trisomy 13
Additional trisomies
- Trisomy 9
- Trisomy 16
- Trisomy 22
Evidence for NIPT is strongest for trisomies 21, 18 and 13. Performance and interpretation differ for rarer trisomies; discuss the expanded screening with your doctor before deciding.
02Sex chromosome screeningSelected differences in sex chromosome number.
Listed conditions
- Turner syndrome — 45,X (XO)
- Klinefelter syndrome — XXY
- Triple-X syndrome — XXX
- Jacobs syndrome — XYY
Discuss the benefits, limitations and your preference for sex chromosome screening with the doctor before testing. Screening can give false-positive or false-negative results.
03Screening across the 23 chromosome pairsAneuploidy means a difference in chromosome number.
Chromosome-number screening
- Aneuploidy screening across the 23 chromosome pairs
This does not mean screening for every genetic condition or every change within a chromosome. The doctor will explain the laboratory’s exact scope, reporting limits and how uncommon findings are followed up.
04Included care & fetal sex informationBrought together in the nett package price.
Ultrasound
- 1 FREE ultrasound scan
- Ultrasound image included
Doctor support
- 2 doctor consultations
- No extra charges for these consultations
Fetal sex information
- Gender identification included
Tell the team if you prefer not to learn the fetal sex. Ask when the scan and consultations will be arranged. Continue the routine antenatal scans recommended by your maternity team.
IS THIS RIGHT FOR ME?
Your pregnancy. Your informed choice.
For expectant mothers from 10 weeks of pregnancy who wish to discuss screening for selected chromosome conditions.
- You would like to understand prenatal screening options.
- You want information about the listed chromosome conditions.
- You have questions about a previous screening result.
- You would value a doctor’s explanation before deciding.
Tell the clinic about twins or other multiple pregnancies, IVF, a vanishing twin, previous screening and relevant medical history. Eligibility and the reportable panel may differ; the doctor will advise which option is appropriate.
BEFORE YOUR VISIT
A little preparation for your appointment.
Discuss the screening scope
Ask what the panel can and cannot detect, including the additional trisomies and sex chromosome screening. Share any questions or reporting preferences before the blood draw.
Check visit instructions
Ask the clinic whether any preparation is needed for your blood sample and ultrasound, including food, water or bladder instructions. Bring your medicine list and follow your clinician’s advice.
Plan the report review
The expected turnaround is seven working days. Ask when this is counted from, how the report will be shared and when your included consultations will take place.
YOUR REPORT & NEXT STEPS
A result, with someone to explain it.
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Discuss & arrange
The doctor explains the screening and confirms suitability. The team arranges the blood sample and included ultrasound.
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Receive your report
Expected in seven working days. The clinic will advise the actual date; an inconclusive sample or laboratory processing issue may take longer.
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Review with the doctor
Two doctor consultations are included in the package. Ask about the review schedule and any further assessment recommended for your result.
QUESTIONS, ANSWERED
Your questions, before you decide.
What does RM1,200 nett include?
The listed chromosome screening, one free ultrasound scan with an image, two doctor consultations and fetal sex information are included. There are no hidden charges for these package items. If separate diagnostic tests or additional care are recommended, the clinic should explain any separate costs before you decide.
When can I have NICC / NIPT?
The package is available from 10 weeks of pregnancy onward, after the doctor confirms pregnancy dating and suitability. Tell the clinic if you are carrying twins, had IVF or have relevant medical or pregnancy history.
Is NIPT a diagnosis?
No. It estimates the chance of the chromosome conditions screened. A high-risk result does not confirm a condition, and a low-risk result does not exclude every condition. Discuss the result with your doctor.
Does screening all 23 chromosome pairs check every condition?
No. Chromosome-number screening is not a complete test of all genes or every chromosome change. Performance also varies by condition. Ask the doctor about the laboratory’s exact panel and the limits of the additional screening.
What happens after a high-risk or inconclusive result?
A high-risk result should be discussed with your doctor, with genetic counselling and confirmatory diagnostic testing considered. An inconclusive result is not a low-risk result and also needs review. Follow-up may include a repeat sample, ultrasound or diagnostic testing, depending on your circumstances.
Do I still need my routine pregnancy scans?
Yes. NIPT does not replace antenatal care or the scans recommended by your maternity team. This package includes one ultrasound with an image; ask the clinic what that scan covers.
Will the report be ready in seven working days?
Seven working days is the expected turnaround. Ask the clinic when the period starts and the anticipated report date. If the laboratory needs further processing or another sample, the team will advise the revised timing.
Is gender identification included?
Fetal sex information is included. If you prefer not to know, tell the clinic before the report is shared. The doctor can explain the reporting limits for your pregnancy.
Do I need to fast or prepare for the ultrasound?
Ask the clinic for the blood-test and ultrasound preparation instructions when booking, including whether any food, water or bladder instructions apply.
WHEN YOU ARE READY
Start with a conversation.
Choose a convenient clinic and ask about NICC / NIPT. The team will help arrange screening and explain the included care.
Browse clinics by area
Clinic guidance requested
Your enquiry goes to MyGP’s central team with the selected package and your clinic preference.
Your nett package total
RM1,200
RM1,200 nett: screening, one ultrasound with image, two doctor consultations and fetal sex information.
No hidden charges for the listed package. Any separate investigations or additional care will be discussed before proceeding. This enquiry does not confirm an appointment.
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NICC / NIPT · 无创产前染色体筛查
孕育新篇章。
您的疑问，值得细心解答。
怀孕带来期待、计划，也带来许多问题。给自己一点时间，在医生说明下了解筛查选择。
怀孕满10周起可考虑的无创产前染色体筛查，配套包含一次超声波及两次医生咨询。
您的 NICC / NIPT 配套
RM1,200
净价 · 列明配套项目无隐藏收费
- 产前染色体筛查
- 一次免费超声波扫描，附图像
- 两次医生咨询 · 胎儿性别信息
诊所会确认适用性、预约时间及预计报告日期。
NIPT 是筛查，不能确诊。医生会在您决定前说明检测范围及可能的后续安排。
怀孕满10周起医生确认适用性
包含两次医生咨询咨询无需额外收费
7个工作日预计报告时间
多一份了解，多一份关怀
一步一步，了解自己的选择。
是否进行产前筛查，是个人的选择。MyGP NICC / NIPT 无创产前染色体筛查，为准妈妈提供胎儿出现特定染色体情况的风险信息，并由医生咨询协助说明检测及结果。
怀孕满10周起可考虑此 RM1,200 净价配套，包含列明的三体、性染色体情况，以及23对染色体数目异常筛查。同时包含一次免费超声波扫描及图像、两次无需额外收费的医生咨询，以及胎儿性别信息。预计报告时间为7个工作日。
NIPT 使用母亲的血液样本进行筛查，不能确诊，也无法排除所有遗传或发育相关问题。医生会说明适用性、检测范围限制及不同结果的意义，协助您在常规产检之外作出知情选择。
配套包含项目
您的筛查，清楚说明。
了解 RM1,200 净价配套内的染色体筛查与医疗服务。
01三体筛查六项列明的三体情况。
常见三体
- 唐氏综合征 — 21三体
- 爱德华氏综合征 — 18三体
- 帕陶氏综合征 — 13三体
其他三体
- 9三体
- 16三体
- 22三体
NIPT 对21、18及13三体的证据最充分。较少见三体的检测表现及解读有所不同，请在决定前与医生讨论扩展筛查。
02性染色体筛查特定性染色体数目差异。
列明情况
- 特纳综合征 — 45,X（XO）
- 克氏综合征 — XXY
- 三X综合征 — XXX
- Jacobs 综合征 — XYY
检测前请与医生讨论性染色体筛查的益处、限制及您的选择。筛查可能出现假阳性或假阴性结果。
0323对染色体数目筛查非整倍体是指染色体数目出现差异。
染色体数目检测
- 23对染色体非整倍体筛查
这不代表能够筛查所有遗传疾病或染色体内部的每一种变化。医生会说明实验室的具体范围、报告限制及少见结果的后续安排。
04已包含的服务及胎儿性别信息整合于配套净价之内。
超声波
- 一次免费超声波扫描
- 附超声波图像
医生支持
- 两次医生咨询
- 这两次咨询无需额外收费
胎儿性别信息
- 已包含性别识别
如不想提前知道胎儿性别，请先告知团队。请询问超声波及咨询的安排，并继续接受产科团队建议的常规孕期检查。
适合我吗？
您的孕期，您的知情选择。
适合怀孕满10周、希望了解特定染色体筛查选择的准妈妈。
- 想了解产前筛查有哪些选择。
- 希望获得列明染色体情况的风险信息。
- 对既往筛查结果有疑问。
- 希望先听医生解释再作决定。
请告知诊所双胎或多胎、试管婴儿、消失性双胎、既往筛查及相关病史。适用性及可报告的项目可能不同，医生会建议合适方案。
体检前须知
到诊前，先了解安排。
确认孕周
带上产检记录及既往孕周超声波报告。医生会确认孕期阶段及满10周起的筛查适用性。
讨论筛查范围
询问哪些情况可以筛查、哪些无法检测，包括其他三体及性染色体筛查。抽血前提出疑问及报告偏好。
确认到诊准备
向诊所询问抽血与超声波的准备要求，包括饮食、饮水或膀胱准备事项。带上用药清单，并遵照医生建议。
安排报告讲解
预计报告时间为7个工作日。请确认从哪天开始计算、如何领取报告，以及两次咨询何时安排。
报告及后续安排
拿到结果，也有人为您说明。
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讨论并安排
医生说明筛查并确认适用性，团队安排抽血及已包含的超声波。
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领取报告
预计7个工作日。诊所会告知具体日期；如样本无法得出明确结果或实验室处理需要更多时间，可能延后。
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与医生讨论
配套包含两次医生咨询。请确认讲解安排，以及根据结果是否建议进一步评估。
常见问题
决定之前，先了解。
RM1,200 净价包含什么？
包含列明的染色体筛查、一次附图像的免费超声波、两次医生咨询及胎儿性别信息。上述配套项目无隐藏收费。如建议进行独立的诊断性检查或额外医疗服务，诊所应先说明相关费用，再由您决定。
什么时候可以做 NICC / NIPT？
怀孕满10周起，经医生确认孕周及适用性后可安排。请告知诊所双胎、试管婴儿或相关健康及孕期情况。
NIPT 可以确诊吗？
不能。它评估所筛查染色体情况的可能性。高风险结果不能确诊，低风险结果也不能排除所有问题，请与医生讨论报告。
检查23对染色体是否代表所有情况都能查出？
不是。染色体数目筛查并非检测全部基因或每一种染色体变化，检测表现也因情况而异。请向医生了解实验室具体范围及扩展筛查的限制。
如果结果高风险或无法得出明确结果怎么办？
高风险结果应由医生解读，并考虑遗传咨询及诊断性检查确认。无法得出明确结果也不等于低风险，需要进一步讨论。医生可能按您的情况建议重新采血、超声波或诊断性检查。
还需要做常规孕期超声波吗？
需要。NIPT 不能取代产检或产科团队建议的超声波。本配套包含一次附图像的超声波，请向诊所确认该次扫描的范围。
报告一定会在7个工作日完成吗？
7个工作日是预计时间。请向诊所确认起算日期及预计领取时间。如实验室需要进一步处理或重新采样，团队会告知调整后的时间。
包含胎儿性别识别吗？
包含胎儿性别信息。如不想知道，请在报告分享前告知诊所。医生可说明适用于您孕期情况的报告限制。
需要空腹或为超声波做准备吗？
预约时请向诊所确认抽血与超声波的准备事项，包括是否有饮食、饮水或膀胱准备要求。
当您准备好时
先从一个咨询开始。
选择方便的诊所，咨询 NICC / NIPT。团队会协助安排筛查，并说明已包含的服务。
按地区查看诊所
请团队协助选择诊所
咨询将发送至 MyGP 团队，并附上所选配套及诊所偏好。
配套净价总额
RM1,200
RM1,200 净价：筛查、一次附图像的超声波、两次医生咨询及胎儿性别信息。
列明配套项目无隐藏收费。如需其他检查或额外医疗服务，会先讨论。发送咨询不代表预约已确认。
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