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. |