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DVL1 Gene Robinow Syndrome Autosomal Dominant Type 2 Genetic Test Cost

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

-21%

The DVL1 Gene Robinow Syndrome Autosomal Dominant Type 2 Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, aimed at identifying mutations in the DVL1 gene. These mutations are responsible for the autosomal dominant form of Robinow Syndrome, a rare genetic disorder characterized by skeletal abnormalities, distinctive facial features, and dental problems. The test plays a crucial role in the early detection and management of the syndrome, allowing for timely intervention and support for affected individuals and their families. The cost of the test is 4400 AED, reflecting the sophisticated technology and expertise required to accurately diagnose this complex condition. By choosing DNA Labs UAE for this test, patients and healthcare providers can expect high-quality services and reliable results, contributing to better health outcomes for those affected by Robinow Syndrome.

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DVL1 Gene Robinow Syndrome Autosomal Dominant Type 2 Genetic Test

At DNA Labs UAE, we offer the DVL1 Gene Robinow Syndrome Autosomal Dominant Type 2 Genetic Test for AED 4400.0.

Test Components

  • DVL1 Gene Robinow syndrome autosomal dominant type 2 Genetic Test

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 DVL1 Gene Robinow syndrome, autosomal dominant type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with DVL1 Gene Robinow syndrome, autosomal dominant type 2 NGS Genetic DNA Test gene DVL1

Test Details

The DVL1 gene is associated with a genetic disorder called Robinow syndrome, specifically the autosomal dominant type 2 form. Robinow syndrome is a rare genetic condition characterized by various physical abnormalities, including distinctive facial features, short stature, and skeletal abnormalities. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously, providing a comprehensive evaluation of an individual’s genetic makeup. In the context of Robinow syndrome, an NGS genetic test can identify mutations or variants in the DVL1 gene that may be responsible for the disorder. By analyzing the DVL1 gene, NGS testing can provide a definitive diagnosis of Robinow syndrome, specifically the autosomal dominant type 2 form. This information can help guide treatment decisions and provide valuable information for genetic counseling and family planning.

Test Name DVL1 Gene Robinow syndrome autosomal dominant type 2 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 DVL1 Gene Robinow syndrome, autosomal dominant type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with DVL1 Gene Robinow syndrome, autosomal dominant type 2 NGS Genetic DNA Test gene DVL1
Test Details

The DVL1 gene is associated with a genetic disorder called Robinow syndrome, specifically the autosomal dominant type 2 form. Robinow syndrome is a rare genetic condition characterized by various physical abnormalities, including distinctive facial features, short stature, and skeletal abnormalities.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously, providing a comprehensive evaluation of an individual’s genetic makeup. In the context of Robinow syndrome, an NGS genetic test can identify mutations or variants in the DVL1 gene that may be responsible for the disorder.

By analyzing the DVL1 gene, NGS testing can provide a definitive diagnosis of Robinow syndrome, specifically the autosomal dominant type 2 form. This information can help guide treatment decisions and provide valuable information for genetic counseling and family planning.

SKU: TEST-4341 Category:

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