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SIX3 Gene Holoprosencephaly Type 2 Genetic Test Cost

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

-21%

The SIX3 Gene Holoprosencephaly Type 2 Genetic Test is a specialized diagnostic procedure aimed at detecting mutations in the SIX3 gene, which are known to cause Holoprosencephaly Type 2, a rare congenital disorder. This condition is characterized by the incomplete development of the brain, leading to significant neurological and facial anomalies. The test involves analyzing the patient’s DNA to identify any genetic alterations in the SIX3 gene that might be responsible for the disorder.

Performed at DNA Labs UAE, a leading facility in genetic diagnostics, this test offers families and individuals crucial information regarding the genetic underpinnings of Holoprosencephaly Type 2. Understanding the genetic basis of the condition can aid in making informed decisions about medical care, potential interventions, and family planning. The cost of the test is 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify mutations in the SIX3 gene.

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SIX3 Gene Holoprosencephaly type 2 Genetic Test

Test Name: SIX3 Gene Holoprosencephaly type 2 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 SIX3 Gene Holoprosencephaly type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SIX3 Gene Holoprosencephaly type 2 NGS Genetic DNA Test gene SIX3

Test Details

The SIX3 gene is a gene that provides instructions for making a protein involved in the development of the brain and face. Mutations in this gene can lead to a condition called holoprosencephaly type 2. Holoprosencephaly is a disorder characterized by the incomplete separation of the brain into two hemispheres. It can result in a range of neurological and facial abnormalities, including intellectual disability, seizures, feeding difficulties, and facial malformations.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. In the context of holoprosencephaly type 2, NGS genetic testing can identify mutations in the SIX3 gene that may be responsible for the condition. By identifying specific mutations in the SIX3 gene, NGS genetic testing can help confirm a diagnosis of holoprosencephaly type 2 and provide information about the likelihood of passing the condition on to future generations. This information can be useful for genetic counseling, family planning, and personalized medical management.

Test Name SIX3 Gene Holoprosencephaly 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 SIX3 Gene Holoprosencephaly type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SIX3 Gene Holoprosencephaly type 2 NGS Genetic DNA Test gene SIX3
Test Details

The SIX3 gene is a gene that provides instructions for making a protein involved in the development of the brain and face. Mutations in this gene can lead to a condition called holoprosencephaly type 2.

Holoprosencephaly is a disorder characterized by the incomplete separation of the brain into two hemispheres. It can result in a range of neurological and facial abnormalities, including intellectual disability, seizures, feeding difficulties, and facial malformations.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. In the context of holoprosencephaly type 2, NGS genetic testing can identify mutations in the SIX3 gene that may be responsible for the condition.

By identifying specific mutations in the SIX3 gene, NGS genetic testing can help confirm a diagnosis of holoprosencephaly type 2 and provide information about the likelihood of passing the condition on to future generations. This information can be useful for genetic counseling, family planning, and personalized medical management.