NIPT or Amniocentesis: What, Why and When?

Рет қаралды 5,422

11 ай бұрын

NIPT (Non-Invasive Prenatal Testing) and amniocentesis are prenatal genetic tests. NIPT analyzes fetal DNA in the mother's blood, providing insights into genetic conditions (mainly Down syndrome, Trisomy 18 and Trisomy 13). Amniocentesis involves extracting amniotic fluid to diagnose chromosomal abnormalities with higher accuracy. Both tests aid informed pregnancy decisions.
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Пікірлер: 20

@deepakkumar7554 5 ай бұрын

Thanks doctor ap ne bahut jaruri अच्छी jankari di

@omusingh5629 Ай бұрын

17 weeks pregnancy nt scan me 7.5 mm and nochal bon dikha nahi kya kre

@NeelamKumari-cb7kb 2 ай бұрын

14:19 mam meri nt scan me result poorly unossified nasal bone aai.then maine double marker karaya usme meri low risk aai then maine anomaly scan karaya usme fir se poorly ossified nasal bone aai.again dr ne mujhe triple marker ke liye blood sample li h .mujhe kya karna chahie yaha pe plss guide me

@JindalIVF Ай бұрын

Kindly contact us at +91 9582-469-429. After reviewing your case, the doctor will provide you with appropriate advice.

@kanadegopal 2 ай бұрын

ma'am meri wife age 24 ki quad marker report me 1:437 risk for down syndrome show kar raha hai...kya hame Amniocentesis test ya nipt test karna chahiye

@JindalIVF Ай бұрын

Kindly contact us at +91 9582-469-429. After reviewing your case, the doctor will provide you with appropriate advice.

@KaranKaran-gj4ik 5 ай бұрын

Mam ager fast report normal hai 2 report normal nhi hai tu kyu krana chya

@JindalIVF 5 ай бұрын

Hi @KaranKaran-gj4ik It depends on the findings of the 2nd report. For any query, you can contact us at: +91 9582-469-429

@cadivyavaswani5274 4 ай бұрын

Ma’am NT is 2.8 (rest all is okay) and if NIPT is low risk, then should we proceed with pregnancy? Or we need to get further tests?

@JindalIVF 4 ай бұрын

Hi @cadivyavaswani5274, This needs consultation with a Fetal medicine specialist. A review of ultrasound images, obstetric and family history is needed for counselling. In some cases, we advise further testing even if NIPT is low risk. For more information you can contact us on +91 9582-469-429.

@mahiranoor5099 3 ай бұрын

@cadiviya do you undergo any further testing

@JindalIVF 3 ай бұрын

Hi,@@mahiranoor5099To know more information you can contact us on +91 9582-469-429.

@nehaanand6973 2 ай бұрын

Kya nipt xxy syndrome accurate batata hai ya fir amniocentesis karana chaiye?

@JindalIVF Ай бұрын

Kindly contact us at +91 9582-469-429. After reviewing your case, the doctor will provide you with appropriate advice.

@subhadranaik7942 18 күн бұрын

Maam Mera nipt test borderline risk aay hai

@dr.ritarathod49 Ай бұрын

Ma'am Mera NIPT test hua hai . Tu Oh please isko Kai padhe kaise

@JindalIVF Ай бұрын

Kindly contact us at +91 9582-469-429 or visit our clinic with your reports: 3050, Dakshin Marg, behind Sri Guru Ravidass Bhawan, Sector 20D, Sector 20, Chandigarh

@stutidhar1990 5 ай бұрын

Maam mera nt scan bilkul normal h..pr T21 1:56 risk show kr rha h 13 week me age risk 1:544 h..kya kru samjh ni aa rha h

@JindalIVF 4 ай бұрын

Hi @stutidhar1990, we will have to review your ultrasound report and family history. You can contact us on +91 9582-469-429 number or visit us at Jindal IVF & Sant Memorial Nursing Home #3050 Sector 20D Chandigarh.

@chaudharyfamilymixvlogs4232 3 ай бұрын

Ab Kaisa h sister baby