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TORCH DNA Detection Test

Original price was: 2,030 د.إ.Current price is: 1,830 د.إ.

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The TORCH DNA Detection Test is a specialized diagnostic procedure conducted at DNA Labs UAE, aimed at identifying infections that could potentially harm unborn babies or newborns. This comprehensive test screens for a group of infections known by the acronym TORCH: Toxoplasmosis, Other agents (like syphilis, varicella-zoster, and parvovirus B19), Rubella, Cytomegalovirus (CMV), and Herpes simplex virus. These infections can lead to severe complications during pregnancy, including birth defects, stillbirth, and neonatal death. By employing advanced DNA testing techniques, the TORCH DNA Detection Test offers highly accurate results, enabling timely intervention and management of these infections to protect both maternal and child health. The cost of this crucial test at DNA Labs UAE is 1830 AED, reflecting the sophisticated technology and expertise required to perform the analysis.

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TORCH DNA Detection Test – Cost, Symptoms, Diagnosis

Welcome to DNA Labs UAE, a leading genetic lab offering the TORCH DNA Detection Test. In this blog, we will discuss the cost, symptoms, and diagnosis of this important test.

Test Details

The TORCH DNA Detection Test is a diagnostic test used to detect the presence of TORCH infections in newborns. TORCH is an acronym that stands for Toxoplasmosis, Other (such as syphilis, varicella-zoster, parvovirus B19), Rubella, Cytomegalovirus, and Herpes simplex virus.

Test Components

  • Toxoplasma
  • Rubella
  • Cytomegalovirus
  • Herpes simplex

Test Price

The cost of the TORCH DNA Detection Test is 1830.0 AED.

Sample Condition

For this test, a sample of 4 mL (2 mL min.) plasma from 1 Lavender top (EDTA) tube OR 3 mL (2 mL min.) CSF/Amniotic fluid in a sterile screw capped container is required. The sample should be shipped refrigerated and should not be frozen.

Report Delivery

The sample should be submitted daily by 11 am, and the report will be delivered within 8 days.

Method

The TORCH DNA Detection Test is performed using the Polymerase Chain Reaction (PCR) method.

Test Type

The TORCH DNA Detection Test is used to detect infections.

Doctor

This test is typically ordered by a Physician or Gynecologist.

Test Department

The TORCH DNA Detection Test is conducted in the Molecular Diagnostics department of our lab.

Pre Test Information

No special preparation is required for this test.

Symptoms and Diagnosis

TORCH infections can be transmitted from mother to fetus during pregnancy and can cause serious health issues in newborns. Common symptoms include fever, rash, jaundice, enlarged liver or spleen, and abnormal neurological findings.

The TORCH DNA Detection Test helps identify the specific TORCH infection causing the symptoms, allowing healthcare providers to provide appropriate treatment and management.

It’s important to note that the TORCH DNA Detection Test is not a routine screening test for all newborns. It is usually performed when there is a suspicion of TORCH infection based on the baby’s symptoms or the mother’s medical history.

Early detection and treatment of TORCH infections can help prevent or minimize complications and long-term health problems in newborns.

Please consult a healthcare provider to order the TORCH DNA Detection Test. The test will be performed in our specialized laboratory.

Test Name TORCH DNA DETECTION Test
Components *Toxoplasma*Rubella*Cytomegalovirus *Herpes simplex
Price 1830.0 AED
Sample Condition 4 mL (2 mL min.) plasma from 1 Lavender top (EDTA) tube OR 3 mL (2 mL min.) CSF\/ Amniotic fluid in a sterile screw capped container. Ship refrigerated. DO NOT FREEZE.
Report Delivery Sample Daily by 11 am; Report 8 days
Method PCR
Test type Infections
Doctor Physician, Gynecologist
Test Department: MOLECULAR DIAGNOSTICS
Pre Test Information No special preparation required
Test Details

The TORCH DNA Detection Test is a diagnostic test used to detect the presence of TORCH infections in newborns. TORCH is an acronym that stands for Toxoplasmosis, Other (such as syphilis, varicella-zoster, parvovirus B19), Rubella, Cytomegalovirus, and Herpes simplex virus. These infections can be transmitted from mother to fetus during pregnancy and can cause serious health issues in newborns.

The TORCH DNA Detection Test involves analyzing the baby’s blood or other body fluids to detect the presence of genetic material (DNA) from these infections. This test is typically performed when a newborn shows symptoms such as fever, rash, jaundice, enlarged liver or spleen, and abnormal neurological findings.

The test can help identify the specific TORCH infection causing the symptoms, allowing healthcare providers to provide appropriate treatment and management. Early detection and treatment of TORCH infections can help prevent or minimize complications and long-term health problems in newborns.

It’s important to note that the TORCH DNA Detection Test is not a routine screening test for all newborns. It is usually performed when there is a suspicion of TORCH infection based on the baby’s symptoms or the mother’s medical history. The test is typically ordered by a healthcare provider and performed in a specialized laboratory.