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RASA1 Gene Parkes Weber Syndrome Genetic Test Cost

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

-21%

The RASA1 Gene Parkes Weber Syndrome Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, aimed at identifying mutations in the RASA1 gene, which are associated with Parkes Weber Syndrome. Parkes Weber Syndrome is a rare congenital condition characterized by a constellation of symptoms including arteriovenous malformations, capillary malformation-arteriovenous malformations, and limb overgrowth. The test is crucial for individuals showing symptoms of the syndrome or those with a family history of the condition, as it can provide definitive genetic evidence of the disorder. Conducted through a blood sample, the analysis focuses on detecting genetic alterations in the RASA1 gene that are known to contribute to the development of this syndrome. The cost of the test is 4400 AED, reflecting the specialized nature of the genetic analysis and the comprehensive insights it offers into the patient’s condition, paving the way for targeted management and treatment strategies.

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RASA1 Gene Parkes Weber Syndrome Genetic Test

At DNA Labs UAE, we offer the RASA1 Gene Parkes Weber Syndrome Genetic Test for individuals suspected to have Parkes Weber syndrome. This genetic disorder is characterized by abnormal blood vessel development, resulting in symptoms like skin discoloration, enlarged veins, and fast-flowing blood vessels.

Test Details

The RASA1 gene is associated with Parkes Weber syndrome. To confirm a diagnosis and identify the specific genetic cause of the condition, we perform Next-Generation Sequencing (NGS) genetic testing. NGS allows for the analysis of multiple genes simultaneously.

Test Components and Price

The RASA1 Gene Parkes Weber Syndrome Genetic Test is priced at 4400.0 AED. The test can be conducted using a blood sample, extracted DNA, or one drop of blood on an FTA card.

Report Delivery

Once the sample is received, the report will be delivered within 3 to 4 weeks.

Method

The RASA1 Gene Parkes Weber Syndrome Genetic Test utilizes NGS technology for accurate and comprehensive analysis.

Test Type

The test falls under the category of Vascular Diseases.

Doctor and Test Department

The test can be ordered by a General Physician and is conducted in our Genetics department.

Pre Test Information

Prior to the test, it is essential to provide the clinical history of the patient. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected by RASA1 Gene Parkes Weber Syndrome.

NGS genetic testing involves sequencing the DNA of an individual and comparing it to a reference genome. This enables the detection of genetic variations within the RASA1 gene, such as point mutations, insertions, or deletions.

The results of the NGS test are crucial for genetic counseling, management, and treatment options for individuals with Parkes Weber syndrome.

Test Name RASA1 Gene Parkes Weber 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 Vascular Diseases
Doctor General Physician
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for RASA1 Gene Parkes Weber syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with RASA1 Gene Parkes Weber syndrome NGS Genetic DNA Test gene RASA1
Test Details

The RASA1 gene is associated with a genetic disorder called Parkes Weber syndrome. Parkes Weber syndrome is a rare condition characterized by the abnormal development of blood vessels, leading to various symptoms including skin discoloration, enlarged veins, and fast-flowing blood vessels.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that can be used to analyze multiple genes simultaneously. In the case of Parkes Weber syndrome, NGS genetic testing can be performed to identify mutations or changes in the RASA1 gene. This can help in confirming a diagnosis of Parkes Weber syndrome and determining the specific genetic cause of the condition.

NGS genetic testing involves sequencing the DNA of an individual and comparing it to a reference genome. This allows for the detection of genetic variations, such as point mutations, insertions, or deletions, within the RASA1 gene. The results of the NGS test can provide important information for genetic counseling, management, and treatment options for individuals with Parkes Weber syndrome.