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DMD Mutation Screening 79 Exons Prenatal Test Cost

Original price was: 4,000 د.إ.Current price is: 3,000 د.إ.

-25%

The “DMD Mutation Screening 79 Exons Prenatal Test” is a specialized genetic examination offered by DNA Labs UAE, designed to identify mutations within the 79 exons of the DMD gene, which is responsible for Duchenne Muscular Dystrophy (DMD). This condition is a severe form of muscular dystrophy that primarily affects boys, leading to progressive muscle degeneration and weakness. Early detection through prenatal testing can provide critical information for expecting parents on the health of their unborn child, allowing for informed decisions and preparation. The test is priced at 3000 AED and utilizes advanced genetic sequencing technologies to accurately screen for the presence of mutations in the DMD gene, ensuring high sensitivity and specificity. DNA Labs UAE, with its state-of-the-art facilities and expert geneticists, ensures a reliable and confidential testing process, making it a trusted choice for prenatal genetic screening.

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DMD Mutation Screening 79 Exons Prenatal Test

Welcome to DNA Labs UAE, a leading genetic lab offering the DMD mutation screening 79 Exons prenatal test at a cost of AED 3000.0.

Test Details

The DMD mutation screening is a genetic test performed during prenatal care to detect mutations in the DMD gene. The DMD gene provides instructions for making a protein called dystrophin, which is essential for muscle function. This test specifically screens for mutations in the 79 exons of the DMD gene. Exons are the coding regions of a gene that contain the instructions for making a protein.

Mutations in these exons can disrupt the production or function of dystrophin, leading to a condition called Duchenne muscular dystrophy (DMD). DMD is an inherited disorder that primarily affects boys, causing progressive muscle weakness and loss of muscle tissue. Symptoms usually appear in early childhood and worsen over time.

The DMD mutation screening test can be performed using different techniques, such as DNA sequencing or multiplex ligation-dependent probe amplification (MLPA). These techniques allow for the detection of specific mutations or changes in the DMD gene.

Components

  • Sterile container
  • Sterile Normal Saline Container
  • EDTA Vacutainer

Price

The cost of the DMD mutation screening 79 Exons prenatal test is AED 3000.0.

Sample Condition

The test can be performed using amniotic fluid, chorionic villi, or cord blood as the sample.

Report Delivery

The report will be delivered within 7-10 days after the test.

Method

The MLPA method is used for the DMD mutation screening 79 Exons prenatal test.

Test Type

The test falls under the category of genetics.

Doctor

The test is performed by our experienced oncology doctors.

Test Department

The DMD mutation screening 79 Exons prenatal test is conducted in our dedicated test department.

Pre Test Information

The DMD mutation screening (79 Exons) prenatal test requires a doctor’s prescription. However, the prescription is not applicable for surgery and pregnancy cases or people planning to travel abroad.

It is important to note that the DMD mutation screening test is specific to the DMD gene and does not screen for other genetic disorders or conditions. Other genetic tests may be recommended based on specific circumstances and family history.

Test Name DMD mutation screening 79 Exons Prenatal Test
Components Sterile container/ Sterile Normal Saline Container/ EDTA Vacutainer
Price 3000.0 AED
Sample Condition Amniotic fluid\/ Chorionic villi\/ Cord Blood
Report Delivery 7-10 days
Method MLPA
Test type Genetics
Doctor Oncology
Test Department:
Pre Test Information DMD mutation screening (79 Exons) Prenatal] can be done with a Doctors prescription. Prescription is not applicable for surgery and pregnancy cases or people planing to travel abroad.
Test Details

DMD mutation screening is a genetic test that is performed during prenatal care to detect mutations in the DMD gene. The DMD gene provides instructions for making a protein called dystrophin, which is essential for muscle function.

The test specifically screens for mutations in the 79 exons of the DMD gene. Exons are the coding regions of a gene that contain the instructions for making a protein. Mutations in these exons can disrupt the production or function of dystrophin, leading to a condition called Duchenne muscular dystrophy (DMD).

DMD is an inherited disorder that primarily affects boys. It causes progressive muscle weakness and loss of muscle tissue. Symptoms usually appear in early childhood and worsen over time.

The DMD mutation screening test can be performed using different techniques, such as DNA sequencing or multiplex ligation-dependent probe amplification (MLPA). These techniques allow for the detection of specific mutations or changes in the DMD gene.

Prenatal DMD mutation screening is typically offered to families with a known history of DMD or when there are signs of the condition in the developing fetus during ultrasound or other prenatal tests. Early detection of DMD mutations can help parents make informed decisions about the pregnancy and plan for the future care of their child.

It is important to note that the DMD mutation screening test is specific to the DMD gene and does not screen for other genetic disorders or conditions. Other genetic tests may be recommended based on the specific circumstances and family history.