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. |
