Prenatal Diagnosis Panel 2 Amniotic Fluid Test sale cost 1000 AED
Herpes Simplex Virus HSV Type 1 and 2 PCR Qualitative Test sale cost 1000 AED Herpes Simplex Virus HSV Type 1 and 2 PCR Qualitative Test Cost 1,300 د.إ Original price was: 1,300 د.إ.1,000 د.إCurrent price is: 1,000 د.إ.
Toxoplasma Qualitative PCR Test sale cost 1000 AED Toxoplasma Qualitative PCR Test Cost 1,300 د.إ Original price was: 1,300 د.إ.1,000 د.إCurrent price is: 1,000 د.إ.
Sale!

Prenatal Diagnosis Panel 2 Amniotic Fluid Test Cost

Original price was: 1,300 د.إ.Current price is: 1,000 د.إ.

-23%

The “Prenatal Diagnosis Panel 2 Amniotic Fluid Test” is a comprehensive diagnostic tool offered by DNA Labs UAE, designed to assess the health and development of a fetus during pregnancy. This test involves the analysis of amniotic fluid, which is the protective liquid surrounding the fetus inside the uterus. The amniotic fluid contains fetal cells and various chemicals produced by the baby, making it a valuable source of genetic material for testing.

The purpose of this panel is to detect genetic abnormalities, infections, and other conditions that might affect the fetus’s development. It can provide vital information about the baby’s health, including the risk of genetic disorders such as Down syndrome, cystic fibrosis, and spina bifida, among others. The test is typically recommended by healthcare providers based on the pregnancy’s risk factors, family history of genetic disorders, or abnormal results from previous prenatal screenings.

Conducted at DNA Labs UAE, a facility known for its advanced genetic testing services, the “Prenatal Diagnosis Panel 2 Amniotic Fluid Test” ensures high accuracy and reliability. The test cost is set at 1000 AED, reflecting the comprehensive nature of the analysis and the valuable insights it provides to expecting parents. This test is a crucial step for those seeking peace of mind and preparing for the needs of their future child, offering a closer look at the baby’s genetic health before birth.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
Guaranteed Safe Checkout

PRENATAL DIAGNOSIS PANEL 2 AMNIOTIC FLUID Test

Test Cost: AED 1000.0

Test Components:

  • Mucopolysaccharidoses (MPS)

Sample Condition:

Submit 10 mL (7 mL min.) Amniotic fluid in a sterile screw capped container. Ship at 18-22°C within 24 hrs. DO NOT FREEZE. Sample should be taken after 16 weeks gestation. Duly filled Prenatal genetic testing consent form (Form 18) is mandatory. Sample to be dispatched with prior appointment.

Report Delivery:

Sample Daily by 4pm; Report within 10 days

Method:

Two-Dimensional electrophoresis

Test Type:

Inborn Errors of Metabolism

Doctor:

Pediatrician

Test Department:

GENETIC

Pre Test Information:

Sample should be taken after 16 weeks gestation. Duly filled Prenatal genetic testing consent form (Form 18) is mandatory. Sample to be dispatched with prior appointment.

Test Details:

The Prenatal Diagnosis Panel 2 Amniotic Fluid Test is a diagnostic test performed on amniotic fluid during pregnancy to screen for various genetic disorders and birth defects in the developing fetus. This test is typically conducted between 15 and 20 weeks of pregnancy and can provide important information about the health of the baby.

The panel includes a comprehensive analysis of the amniotic fluid sample, which can detect chromosomal abnormalities such as Down syndrome (trisomy 21), Edwards syndrome (trisomy 18), and Patau syndrome (trisomy 13). It can also identify other genetic disorders like cystic fibrosis, sickle cell disease, and spinal muscular atrophy. In addition to genetic disorders, the panel can screen for neural tube defects such as spina bifida and anencephaly. It can also detect certain metabolic disorders and assess the baby’s lung maturity.

The Prenatal Diagnosis Panel 2 Amniotic Fluid Test involves extracting a small amount of amniotic fluid from the womb through a needle inserted into the abdomen. The fluid is then analyzed in a laboratory using various techniques, including chromosome analysis, DNA testing, and biochemical assays.

It is important to note that this test is an invasive procedure and carries a small risk of complications, including infection or injury to the fetus. Therefore, it is typically recommended for women with a higher risk of having a baby with a genetic disorder or birth defect, such as those with a family history of genetic conditions or advanced maternal age.

The results of the test can help expectant parents make informed decisions about their pregnancy, including potential treatment options, further diagnostic tests, or preparation for the birth of a child with special needs. It is important to consult with a healthcare provider or genetic counselor to understand the implications of the test results and discuss any concerns or questions.

Test Name PRENATAL DIAGNOSIS PANEL 2 AMNIOTIC FLUID Test
Components *Mucopolysaccharidoses(MPS)
Price 1000.0 AED
Sample Condition Submit 10 mL (7 mL min.) Amniotic fluid in a sterile screw capped container.Shipat18\u0192??22?\u00f8Cwithin24 hrs. DO NOT FREEZE. Sample should betakenafter16weeksgestation. Duly filled Prenatal genetic testing consent form (Form 18) is mandatory. Sample to be dispatched with prior appointment.
Report Delivery SampleDailyby4pm;Report10days
Method TwoDimensionalelectrophoresis
Test type Inborn Errors of Metabolism
Doctor Pediatrician
Test Department: GENETIC
Pre Test Information Sample should betakenafter16weeksgestation. Duly filled Prenatal genetic testing consent form (Form 18) is mandatory. Sample to be dispatched with prior appointment.
Test Details

The Prenatal Diagnosis Panel 2 Amniotic Fluid Test is a diagnostic test performed on amniotic fluid during pregnancy to screen for various genetic disorders and birth defects in the developing fetus. This test is typically conducted between 15 and 20 weeks of pregnancy and can provide important information about the health of the baby.

The panel includes a comprehensive analysis of the amniotic fluid sample, which can detect chromosomal abnormalities such as Down syndrome (trisomy 21), Edwards syndrome (trisomy 18), and Patau syndrome (trisomy 13). It can also identify other genetic disorders like cystic fibrosis, sickle cell disease, and spinal muscular atrophy.

In addition to genetic disorders, the panel can screen for neural tube defects such as spina bifida and anencephaly. It can also detect certain metabolic disorders and assess the baby’s lung maturity.

The Prenatal Diagnosis Panel 2 Amniotic Fluid Test involves extracting a small amount of amniotic fluid from the womb through a needle inserted into the abdomen. The fluid is then analyzed in a laboratory using various techniques, including chromosome analysis, DNA testing, and biochemical assays.

It is important to note that this test is an invasive procedure and carries a small risk of complications, including infection or injury to the fetus. Therefore, it is typically recommended for women with a higher risk of having a baby with a genetic disorder or birth defect, such as those with a family history of genetic conditions or advanced maternal age.

The results of the test can help expectant parents make informed decisions about their pregnancy, including potential treatment options, further diagnostic tests, or preparation for the birth of a child with special needs. It is important to consult with a healthcare provider or genetic counselor to understand the implications of the test results and discuss any concerns or questions.

SKU: TEST-5693