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.