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PROM1 Gene Cone-Rod Dystrophy Type 12 Genetic Test Cost

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

-21%

The PROM1 Gene Cone-Rod Dystrophy Type 12 Genetic Test is a specialized diagnostic procedure aimed at identifying mutations in the PROM1 gene, which are implicated in the development of Cone-Rod Dystrophy Type 12 (CRD12). This condition is a form of inherited eye disorder that primarily affects the cone and rod cells of the retina, leading to progressive vision loss. The test is crucial for individuals with a family history of CRD12 or those exhibiting symptoms of the disorder, as it provides a definitive diagnosis by analyzing the genetic makeup for specific anomalies in the PROM1 gene.

Performed at DNA Labs UAE, a reputable facility known for its advanced genetic testing services, the test involves collecting a DNA sample, usually through a blood draw or cheek swab. The sample is then subjected to comprehensive genetic analysis to detect any mutations associated with CRD12. This information is vital for understanding the risk of developing the condition, potential progression, and guiding decisions regarding management and treatment options.

The cost of the PROM1 Gene Cone-Rod Dystrophy Type 12 Genetic Test at DNA Labs UAE is set at 4400 AED. While the price may seem significant, the value of the information it provides cannot be overstated for affected individuals and their families. It offers a path towards personalized care strategies and, in some cases, might inform decisions about family planning.

Description

PROM1 Gene Cone-rod dystrophy type 12 Genetic Test

Test Name: PROM1 Gene Cone-rod dystrophy type 12 Genetic Test

Components: DNA Labs UAE

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 PROM1 Gene Cone-rod dystrophy type 12 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PROM1 Gene Cone-rod dystrophy type 12 NGS Genetic DNA Test gene PROM1

Test Details: The PROM1 gene is associated with cone-rod dystrophy type 12, a rare genetic disorder that affects the retina of the eye. This condition causes progressive vision loss, starting with the central vision and eventually affecting the peripheral vision. The PROM1 gene provides instructions for making a protein called prominin-1, which is found in the photoreceptor cells of the retina. Mutations in the PROM1 gene can disrupt the normal function of the protein, leading to the degeneration of the photoreceptor cells and the development of cone-rod dystrophy type 12. NGS (next-generation sequencing) genetic testing can be used to identify mutations in the PROM1 gene that are associated with cone-rod dystrophy type 12. This type of testing uses advanced DNA sequencing technology to analyze multiple genes simultaneously, allowing for more comprehensive and accurate testing. NGS genetic testing can help diagnose cone-rod dystrophy type 12 in individuals with symptoms of the condition and can also be used for carrier testing in family members of affected individuals. Genetic testing can also provide valuable information for genetic counseling and family planning.

Test Name	PROM1 Gene Cone-rod dystrophy type 12 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 PROM1 Gene Cone-rod dystrophy type 12 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PROM1 Gene Cone-rod dystrophy type 12 NGS Genetic DNA Test gene PROM1
Test Details	The PROM1 gene is associated with cone-rod dystrophy type 12, a rare genetic disorder that affects the retina of the eye. This condition causes progressive vision loss, starting with the central vision and eventually affecting the peripheral vision. The PROM1 gene provides instructions for making a protein called prominin-1, which is found in the photoreceptor cells of the retina. Mutations in the PROM1 gene can disrupt the normal function of the protein, leading to the degeneration of the photoreceptor cells and the development of cone-rod dystrophy type 12. NGS (next-generation sequencing) genetic testing can be used to identify mutations in the PROM1 gene that are associated with cone-rod dystrophy type 12. This type of testing uses advanced DNA sequencing technology to analyze multiple genes simultaneously, allowing for more comprehensive and accurate testing. NGS genetic testing can help diagnose cone-rod dystrophy type 12 in individuals with symptoms of the condition and can also be used for carrier testing in family members of affected individuals. Genetic testing can also provide valuable information for genetic counseling and family planning.