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ZIC2 Gene Holoprosencephaly Type 5 Genetic Test

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

-21%

The “ZIC2 Gene Holoprosencephaly Type 5 Genetic Test” is a specialized diagnostic examination aimed at identifying mutations in the ZIC2 gene, which are linked to Holoprosencephaly Type 5 (HPE5), a rare congenital disorder characterized by the incomplete development of the brain. This condition can result in a spectrum of facial anomalies, intellectual disabilities, and, in severe cases, an inability for the brain to divide into two hemispheres. Given the genetic nature of HPE5, the test is crucial for families with a history of the disorder, offering them a chance to understand their genetic makeup, assess risks for future offspring, and plan for medical management or interventions.

The test is conducted at DNA Labs UAE, a facility known for its state-of-the-art genetic testing services. With a focus on accuracy and confidentiality, DNA Labs UAE employs advanced genomic technologies to provide reliable results. The cost of the test is 4400 AED, reflecting the intricate processes and expertise required to detect the specific gene mutations associated with HPE5. By opting for this test, individuals and families can gain valuable insights into their genetic health, empowering them to make informed decisions regarding their well-being and future family planning.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
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ZIC2 Gene Holoprosencephaly type 5 Genetic Test

Welcome to DNA Labs UAE, where we offer the ZIC2 Gene Holoprosencephaly type 5 Genetic Test. This test is designed to diagnose individuals with holoprosencephaly type 5, a condition characterized by abnormal brain development. By analyzing the ZIC2 gene using NGS genetic testing, we can identify any mutations or variations that may be associated with this disorder.

Test Components and Price

The ZIC2 Gene Holoprosencephaly type 5 Genetic Test costs 4400.0 AED. The test requires a blood or extracted DNA sample, or one drop of blood on an FTA card.

Report Delivery and Method

After the sample is collected, the report will be delivered within 3 to 4 weeks. The test utilizes NGS (Next Generation Sequencing) technology, which allows for the simultaneous sequencing of multiple genes or even the entire genome.

Test Type and Doctor

The ZIC2 Gene Holoprosencephaly type 5 Genetic Test falls under the category of Dysmorphology. It is recommended for individuals seeking diagnosis and management of this condition to consult with a Pediatrics doctor.

Test Department and Pre-Test Information

The ZIC2 Gene Holoprosencephaly type 5 Genetic Test is conducted in our Genetics department. Before undergoing the test, it is important to provide the clinical history of the patient. Additionally, a Genetic Counselling session is recommended to draw a pedigree chart of family members affected by ZIC2 Gene Holoprosencephaly type 5 NGS Genetic DNA Test gene ZIC2.

Test Details

The ZIC2 gene is associated with holoprosencephaly type 5, a disorder characterized by abnormal brain development. This condition results in the failure of the brain to divide into two hemispheres, leading to various neurological and physical abnormalities.

NGS genetic testing is a more advanced and efficient method compared to traditional Sanger sequencing. By analyzing the ZIC2 gene using NGS techniques, we can identify any mutations or variations that may contribute to the development of holoprosencephaly type 5.

Collecting a blood or saliva sample from the individual, isolating the DNA, and sequencing the gene using NGS techniques are involved in the ZIC2 Gene Holoprosencephaly type 5 Genetic Test. The results of the test will be analyzed to determine if there are any mutations or variations in the ZIC2 gene.

Please note that genetic testing for holoprosencephaly type 5 and other genetic conditions should be performed and interpreted by qualified healthcare professionals, such as geneticists or genetic counselors, who can provide appropriate guidance and support based on the test results.

Test Name ZIC2 Gene Holoprosencephaly type 5 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 ZIC2 Gene Holoprosencephaly type 5 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ZIC2 Gene Holoprosencephaly type 5 NGS Genetic DNA Test gene ZIC2
Test Details

The ZIC2 gene is associated with a condition called holoprosencephaly type 5. Holoprosencephaly is a disorder characterized by abnormal brain development, specifically the failure of the brain to divide into two hemispheres. This can result in a range of neurological and physical abnormalities.

NGS (Next Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous sequencing of multiple genes or even the entire genome. It is a more advanced and efficient method compared to traditional Sanger sequencing.

The ZIC2 gene can be analyzed using NGS genetic testing to identify any mutations or variations in the gene that may be associated with holoprosencephaly type 5. This can help in diagnosing individuals with the condition and provide valuable information for genetic counseling and management of the disorder.

NGS genetic testing for the ZIC2 gene may involve collecting a blood or saliva sample from the individual, isolating the DNA, and sequencing the gene using NGS techniques. The results of the test can then be analyzed to determine if there are any mutations or variations in the ZIC2 gene that may be contributing to the development of holoprosencephaly type 5.

It is important to note that genetic testing for holoprosencephaly type 5 and other genetic conditions should be performed and interpreted by qualified healthcare professionals, such as geneticists or genetic counselors, who can provide appropriate guidance and support based on the test results.