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ROR2 Gene Robinow Syndrome Autosomal Recessive Genetic Test Cost

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

-21%

Robinow Syndrome is a rare genetic disorder characterized by skeletal dysplasia, which includes short stature, limb shortening, genital hypoplasia, and facial abnormalities. The ROR2 gene plays a crucial role in the development of the skeletal and genital systems, and mutations in this gene are associated with the autosomal recessive form of Robinow Syndrome. Identifying mutations in the ROR2 gene can confirm a diagnosis of Robinow Syndrome and help in understanding the condition’s severity and potential management strategies.

At DNA Labs UAE, individuals can undergo a genetic test specifically designed to identify mutations in the ROR2 gene, which is pivotal for diagnosing autosomal recessive Robinow Syndrome. The test is comprehensive and ensures accuracy in detecting the genetic anomaly responsible for the syndrome.

The cost of the ROR2 Gene Robinow Syndrome Autosomal Recessive Genetic Test at DNA Labs UAE is 4400 AED. This test is a valuable resource for families seeking answers about this rare condition, enabling informed decisions regarding health and family planning. It’s important to note that consultation with a healthcare provider or a genetic counselor is recommended to interpret the test results accurately and to understand the implications for the individual and their family.

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ROR2 Gene Robinow Syndrome Autosomal Recessive Genetic Test

Welcome to DNA Labs UAE, where we offer the ROR2 Gene Robinow Syndrome Autosomal Recessive Genetic Test. This test can help diagnose and provide information about the specific genetic mutation involved in Robinow syndrome, a rare genetic disorder characterized by distinctive facial features, short stature, limb abnormalities, and other skeletal abnormalities.

Test Details

The ROR2 Gene Robinow Syndrome Autosomal Recessive Genetic Test is a type of genetic test that uses Next-Generation Sequencing (NGS) technology. NGS technology allows us to analyze multiple genes simultaneously, providing comprehensive results. The test specifically identifies mutations or variations in the ROR2 gene, which is associated with Robinow syndrome.

Test Components and Price

The price for the ROR2 Gene Robinow Syndrome Autosomal Recessive Genetic Test is 4400.0 AED. The test requires a sample condition of either blood, 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. Our team of experts will carefully analyze the results and provide a detailed report.

Method

The ROR2 Gene Robinow Syndrome Autosomal Recessive Genetic Test utilizes NGS technology, which allows for efficient and accurate analysis of the ROR2 gene.

Test Type

The test falls under the category of dysmorphology, as it focuses on identifying genetic mutations associated with physical abnormalities and developmental disorders.

Doctor and Test Department

The ROR2 Gene Robinow Syndrome Autosomal Recessive Genetic Test is conducted by our experienced team of pediatric doctors in the Genetics department.

Pre Test Information

Prior to the test, it is important to provide the clinical history of the patient who is going for the ROR2 Gene Robinow Syndrome Autosomal Recessive Genetic Test. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by the disorder.

About Robinow Syndrome

Robinow syndrome is a rare genetic disorder that is inherited in an autosomal recessive manner. This means that both copies of the ROR2 gene, one inherited from each parent, must have a mutation for an individual to be affected by the disorder. In addition to the distinctive facial features, short stature, and limb abnormalities, Robinow syndrome can also affect other body systems, including the heart, kidneys, and genitals.

Importance of Genetic Testing

Genetic testing can help confirm a diagnosis of Robinow syndrome and provide valuable information about the specific genetic mutation involved. It is crucial to note that genetic testing should always be performed and interpreted by a qualified healthcare professional or genetic counselor. They can offer guidance and support in understanding the results and their implications for the individual and their family.

At DNA Labs UAE, we are dedicated to providing accurate and reliable genetic testing services. If you suspect Robinow syndrome or have any concerns about your genetic health, we encourage you to consult with our experts. Contact us today to schedule an appointment or to learn more about our services.

Test Name ROR2 Gene Robinow syndrome autosomal recessive 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 ROR2 Gene Robinow syndrome, autosomal recessive NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ROR2 Gene Robinow syndrome, autosomal recessive NGS Genetic DNA Test gene ROR2
Test Details

ROR2 Gene Robinow syndrome is a genetic disorder that is inherited in an autosomal recessive manner. Autosomal recessive means that both copies of the gene, one inherited from each parent, must have a mutation for the individual to be affected by the disorder.

NGS (Next-Generation Sequencing) Genetic Test is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. This test can identify mutations or variations in the ROR2 gene, which is associated with Robinow syndrome.

Robinow syndrome is a rare genetic disorder characterized by distinctive facial features, short stature, limb abnormalities, and other skeletal abnormalities. It can also affect other body systems, including the heart, kidneys, and genitals. Genetic testing can help confirm a diagnosis of Robinow syndrome and provide information about the specific genetic mutation involved.

It is important to note that genetic testing should be performed and interpreted by a qualified healthcare professional or genetic counselor. They can provide guidance and support in understanding the results and their implications for the individual and their family.