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CHM Gene Choroideremia Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The CHM Gene Choroideremia Genetic Test is a specialized diagnostic procedure offered at DNA Labs UAE, designed to identify mutations in the CHM gene, which are linked to the development of choroideremia. Choroideremia is a rare genetic condition that causes progressive vision loss, typically affecting males due to its X-linked inheritance pattern. This condition leads to the degeneration of the choroid, retinal pigment epithelium, and the photoreceptors.

The test is critical for individuals with a family history of choroideremia, offering them an opportunity for early diagnosis. Early identification of the condition can aid in better management and understanding of the disease progression, and potentially guide treatment decisions in the future. Furthermore, it serves an essential role in genetic counseling, helping families understand the risk of passing the condition to future generations.

Performed at the state-of-the-art facilities of DNA Labs UAE, the test requires a DNA sample, usually collected through a blood draw or cheek swab. The process is meticulous, ensuring accuracy and confidentiality of the genetic information.

The cost of the CHM Gene Choroideremia Genetic Test at DNA Labs UAE is 4400 AED. While the price may seem substantial, the value of the information it provides for affected individuals and their families is significant, offering insights into managing the condition and making informed decisions about family planning.

Description

CHM Gene Choroideremia Genetic Test

Are you or your family members experiencing symptoms of choroideremia? DNA Labs UAE offers the CHM Gene Choroideremia Genetic Test to help diagnose this genetic condition and provide valuable information for genetic counseling and reproductive decisions.

Test Details

The CHM gene is associated with choroideremia, an X-linked recessive disorder that primarily affects the retina and leads to progressive vision loss. Our NGS (Next-Generation Sequencing) technology allows us to analyze multiple genes simultaneously, including the CHM gene.

Components

Test Name: CHM Gene Choroideremia Genetic Test
Price: 4400.0 AED
Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery: 3 to 4 Weeks
Method: NGS Technology
Test Type: Dysmorphology
Doctor: Pediatrics
Test Department: Genetics

Pre Test Information

Prior to undergoing the CHM Gene Choroideremia Genetic Test, a clinical history of the patient is required. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by the CHM gene mutation.

How the Test Works

The CHM Gene Choroideremia Genetic Test involves obtaining a DNA sample, typically through a blood sample, from the individual being tested. The DNA is then sequenced using NGS technology to identify any variations or mutations in the CHM gene. The results of the test can help confirm a diagnosis of choroideremia and provide information about the specific genetic changes involved.

Benefits of Genetic Testing

Genetic testing for choroideremia can be beneficial for individuals with symptoms of the condition, as well as their family members who may be at risk of carrying the CHM gene mutation. It can aid in making an accurate diagnosis, providing genetic counseling, and informing reproductive decisions.

Importance of Professional Guidance

It’s important to note that genetic testing for choroideremia should be conducted by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate guidance and support.

Don’t let the symptoms of choroideremia go undiagnosed. Contact DNA Labs UAE today to schedule your CHM Gene Choroideremia Genetic Test and take control of your genetic health.

Test Name	CHM Gene Choroideremia Genetic Test
Components
Price	4400.0 AED
Sample Condition	Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery	3 to 4 Weeks
Method	NGS Technology
Test type	Dysmorphology
Doctor	Pediatrics
Test Department:	Genetics
Pre Test Information	Clinical History of Patient who is going for CHM Gene Choroideremia NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CHM Gene Choroideremia NGS Genetic DNA Test gene CHM
Test Details	The CHM gene is associated with a genetic condition called choroideremia. Choroideremia is an X-linked recessive disorder that primarily affects the retina, leading to progressive vision loss. NGS (Next-Generation Sequencing) is a high-throughput DNA sequencing technology that can analyze multiple genes simultaneously. In the context of choroideremia, an NGS genetic test can identify mutations or variants in the CHM gene that may be responsible for the condition. This genetic test involves obtaining a DNA sample, typically through a blood sample, from the individual being tested. The DNA is then sequenced using NGS technology to identify any variations or mutations in the CHM gene. The results of the test can help confirm a diagnosis of choroideremia and provide information about the specific genetic changes involved. Genetic testing for choroideremia can be helpful for individuals with symptoms of the condition, as well as their family members who may be at risk of carrying the CHM gene mutation. It can aid in making an accurate diagnosis, providing genetic counseling, and informing reproductive decisions. It’s important to note that genetic testing for choroideremia should be conducted by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate guidance and support.

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