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TRPV3 Gene Olmsted Syndrome Genetic Test Cost

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

-21%

The TRPV3 Gene Olmsted Syndrome Genetic Test is a specialized diagnostic tool used to detect mutations in the TRPV3 gene, which are associated with Olmsted Syndrome. Olmsted Syndrome is a rare genetic disorder characterized by severe skin abnormalities, including palmoplantar keratoderma (thickening of the skin on the palms and soles) and periorificial keratotic plaques. It can also affect hair, teeth, and nails, and in some cases, cause other systemic symptoms.

The test is conducted at DNA Labs UAE, a leading facility for genetic and molecular diagnostics in the United Arab Emirates. The procedure involves collecting a DNA sample, usually through a blood draw or a cheek swab, which is then analyzed to identify any mutations in the TRPV3 gene that are indicative of Olmsted Syndrome.

The cost of the TRPV3 Gene Olmsted Syndrome Genetic Test at DNA Labs UAE is 4400 AED. This cost includes the collection of the sample, the genetic analysis, and a comprehensive report that explains the results. The report is crucial for guiding treatment decisions, informing clinical management, and offering genetic counseling to affected families. This test is a vital resource for individuals exhibiting symptoms of Olmsted Syndrome or those with a family history of the disorder, aiming to confirm a diagnosis and facilitate appropriate care and management.

Description

TRPV3 Gene Olmsted syndrome Genetic Test

At DNA Labs UAE, we offer the TRPV3 Gene Olmsted syndrome Genetic Test at a cost of AED 4400.0.

Test Details

The TRPV3 gene is responsible for encoding a protein called transient receptor potential cation channel subfamily V member 3. Mutations in this gene have been associated with a rare genetic disorder called Olmsted syndrome. Olmsted syndrome is a rare genetic disorder characterized by the development of thickened, keratinized skin on the palms of the hands and soles of the feet. This condition can cause significant pain and discomfort, as well as other complications such as hair loss, nail abnormalities, and eye problems.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously, allowing for the detection of mutations or variations in the DNA sequence. In the case of Olmsted syndrome, NGS genetic testing can be used to identify mutations in the TRPV3 gene that may be responsible for the development of the condition. By identifying specific mutations in the TRPV3 gene, NGS genetic testing can provide a definitive diagnosis of Olmsted syndrome. This information can be crucial for understanding the underlying cause of the disorder, predicting disease progression, and potentially developing targeted treatment options.

It is important to note that NGS genetic testing should be performed by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate genetic counseling and guidance.

Test Components and Price

Test Name: TRPV3 Gene Olmsted syndrome Genetic Test
Components: NGS Technology
Price: 4400.0 AED
Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery: 3 to 4 Weeks
Test Type: Dysmorphology
Doctor: Pediatrics
Test Department: Genetics

Pre Test Information

Clinical History of Patient who is going for TRPV3 Gene Olmsted syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TRPV3 Gene Olmsted syndrome NGS Genetic DNA Test gene TRPV3.

Test Name	TRPV3 Gene Olmsted syndrome 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 TRPV3 Gene Olmsted syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TRPV3 Gene Olmsted syndrome NGS Genetic DNA Test gene TRPV3
Test Details	The TRPV3 gene is responsible for encoding a protein called transient receptor potential cation channel subfamily V member 3. Mutations in this gene have been associated with a rare genetic disorder called Olmsted syndrome. Olmsted syndrome is a rare genetic disorder characterized by the development of thickened, keratinized skin on the palms of the hands and soles of the feet. This condition can cause significant pain and discomfort, as well as other complications such as hair loss, nail abnormalities, and eye problems. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously, allowing for the detection of mutations or variations in the DNA sequence. In the case of Olmsted syndrome, NGS genetic testing can be used to identify mutations in the TRPV3 gene that may be responsible for the development of the condition. By identifying specific mutations in the TRPV3 gene, NGS genetic testing can provide a definitive diagnosis of Olmsted syndrome. This information can be crucial for understanding the underlying cause of the disorder, predicting disease progression, and potentially developing targeted treatment options. It is important to note that NGS genetic testing should be performed by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate genetic counseling and guidance.