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PITPNM3 Gene Cone-Rod Dystrophy Type 5 Genetic Test

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

-21%

The PITPNM3 gene is associated with Cone-Rod Dystrophy Type 5 (CORD5), a rare genetic disorder that affects the retina and leads to progressive vision loss. The disorder primarily impacts the cone and rod photoreceptor cells in the eye, which are crucial for color vision, central vision, and low-light vision. Mutations in the PITPNM3 gene disrupt the normal function of these cells, leading to the symptoms of CORD5.

To diagnose this condition, genetic testing can be conducted to identify mutations in the PITPNM3 gene. DNA Labs UAE offers a specific genetic test for this purpose, providing a crucial diagnostic tool for individuals exhibiting symptoms of Cone-Rod Dystrophy Type 5 or those with a family history of the disorder. The test involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory for the presence of genetic mutations associated with the condition.

The cost of the PITPNM3 gene Cone-Rod Dystrophy Type 5 genetic test at DNA Labs UAE is 4400 AED. This investment can provide invaluable information for affected individuals and their families, enabling them to understand their condition better, consider their options for genetic counseling, and plan for any necessary adjustments to their lifestyle or healthcare management.

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PITPNM3 Gene Cone-rod dystrophy type 5 Genetic Test

Are you concerned about Cone-rod dystrophy type 5 (CORD5)? DNA Labs UAE offers a comprehensive genetic test for the PITPNM3 gene, which is associated with this rare genetic disorder. Read on to learn more about the test and its benefits.

Test Components and Price

The PITPNM3 Gene Cone-rod dystrophy type 5 Genetic Test is available at a cost of AED 4400.0. The test requires a blood sample or extracted DNA, or simply one drop of blood on an FTA Card.

Report Delivery and Method

After the sample is collected, the report will be delivered within 3 to 4 weeks. The test utilizes NGS (Next-Generation Sequencing) technology, which allows for a detailed analysis of the DNA sequence of the PITPNM3 gene.

Test Type and Doctor

This genetic test falls under the category of Ophthalmology Disorders. It is recommended to consult an Ophthalmologist for this test.

Test Department and Pre Test Information

The test is conducted by the Genetics department of DNA Labs UAE. Prior to the test, it is important to provide the clinical history of the patient who is undergoing the PITPNM3 Gene Cone-rod dystrophy type 5 NGS Genetic DNA Test. A Genetic Counselling session will also be conducted to draw a pedigree chart of family members affected by CORD5.

About the PITPNM3 Gene and CORD5

The PITPNM3 gene is associated with Cone-rod dystrophy type 5 (CORD5), a rare genetic disorder that affects the cells in the retina responsible for color vision and visual acuity. By analyzing the DNA sequence of the PITPNM3 gene, NGS genetic testing can detect any mutations or variations that may be associated with CORD5.

Benefits of the Test

The PITPNM3 Gene Cone-rod dystrophy type 5 Genetic Test can help in the diagnosis of individuals with CORD5. It can also predict the risk of passing the condition on to offspring, and provide valuable information for genetic counseling and management of the disease.

Test Name PITPNM3 Gene Cone-rod dystrophy type 5 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 Ophthalmology Disorders
Doctor Ophthalmologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for PITPNM3 Gene Cone-rod dystrophy type 5 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PITPNM3 Gene Cone-rod dystrophy type 5 NGS Genetic DNA Test gene PITPNM3
Test Details

The PITPNM3 gene is associated with cone-rod dystrophy type 5 (CORD5), a rare genetic disorder that affects the cells in the retina responsible for color vision and visual acuity. NGS genetic testing can be used to analyze the DNA sequence of the PITPNM3 gene and detect any mutations or variations that may be associated with CORD5. This test can help diagnose individuals with CORD5, predict the risk of passing the condition on to offspring, and provide information for genetic counseling and management of the disease.