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VSX1 Gene Craniofacial Anomalies and Anterior Segment Dysgenesis Syndrome Genetic Test Cost

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

-21%

The VSX1 Gene Craniofacial Anomalies and Anterior Segment Dysgenesis Syndrome Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the VSX1 gene. These mutations are associated with a range of conditions, including craniofacial anomalies and anterior segment dysgenesis syndrome, which can lead to significant visual impairment. The test is crucial for individuals exhibiting symptoms of these conditions or those with a family history, as it provides essential information for accurate diagnosis, management, and treatment planning.

Performed in the state-of-the-art facilities of DNA Labs UAE, the test ensures high accuracy and reliability. The cost of the test is 4400 AED, which reflects the sophisticated technology and expertise required to analyze genetic variations accurately. By opting for this genetic test, patients and healthcare providers can make informed decisions regarding the care and intervention strategies to manage or mitigate the impact of these genetic disorders.

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VSX1 Gene Craniofacial anomalies and anterior segment dysgenesis syndrome Genetic Test

Test Name: VSX1 Gene Craniofacial anomalies and anterior segment dysgenesis syndrome Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

Price: 4400.0 AED

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 VSX1 Gene Craniofacial anomalies and anterior segment dysgenesis syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with VSX1 Gene Craniofacial anomalies and anterior segment dysgenesis syndrome NGS Genetic DNA Test gene VSX1

Test Details: The VSX1 gene is associated with a condition called craniofacial anomalies and anterior segment dysgenesis syndrome. This syndrome is characterized by abnormal development of the craniofacial region (head and face) and the anterior segment of the eye. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that can be used to analyze multiple genes simultaneously. In the context of craniofacial anomalies and anterior segment dysgenesis syndrome, NGS genetic testing can be used to identify mutations or variations in the VSX1 gene. This genetic test can help in the diagnosis of the syndrome and provide information about the specific genetic changes that are contributing to the condition. It can also be used for genetic counseling and to assess the risk of passing the syndrome on to future generations. Overall, NGS genetic testing for the VSX1 gene can play an important role in the diagnosis and management of craniofacial anomalies and anterior segment dysgenesis syndrome.

Test Name VSX1 Gene Craniofacial anomalies and anterior segment dysgenesis 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 Dysmorphology
Doctor Pediatrics
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for VSX1 Gene Craniofacial anomalies and anterior segment dysgenesis syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with VSX1 Gene Craniofacial anomalies and anterior segment dysgenesis syndrome NGS Genetic DNA Test gene VSX1
Test Details

The VSX1 gene is associated with a condition called craniofacial anomalies and anterior segment dysgenesis syndrome. This syndrome is characterized by abnormal development of the craniofacial region (head and face) and the anterior segment of the eye.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that can be used to analyze multiple genes simultaneously. In the context of craniofacial anomalies and anterior segment dysgenesis syndrome, NGS genetic testing can be used to identify mutations or variations in the VSX1 gene.

This genetic test can help in the diagnosis of the syndrome and provide information about the specific genetic changes that are contributing to the condition. It can also be used for genetic counseling and to assess the risk of passing the syndrome on to future generations.

Overall, NGS genetic testing for the VSX1 gene can play an important role in the diagnosis and management of craniofacial anomalies and anterior segment dysgenesis syndrome.

SKU: TEST-4073 Category:

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