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KCNH1 Gene Temple-Baraitser Syndrome Genetic Test Cost

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

-21%

The KCNH1 Gene Temple-Baraitser Syndrome Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the KCNH1 gene, which are linked to Temple-Baraitser Syndrome (TBS). TBS is a rare genetic disorder characterized by intellectual disability, epilepsy, distinct facial features, and abnormalities of the hands and feet. The test involves analyzing the patient’s DNA to detect specific genetic alterations in the KCNH1 gene, providing crucial information for accurate diagnosis, management, and genetic counseling for affected families.

The test is priced at 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify mutations in the KCNH1 gene. Conducted in the state-of-the-art facilities of DNA Labs UAE, this genetic test is a critical tool for healthcare providers in the diagnosis and treatment planning for individuals suspected of having Temple-Baraitser Syndrome. The result from this test not only aids in confirming the diagnosis but also helps in understanding the genetic basis of the condition, which can be vital for family planning and understanding the risk of recurrence in future pregnancies.

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KCNH1 Gene Temple-Baraitser syndrome Genetic Test

Introduction

At DNA Labs UAE, we offer the KCNH1 Gene Temple-Baraitser syndrome Genetic Test, which is designed to diagnose Temple-Baraitser syndrome, a rare genetic disorder. This blog post provides detailed information about the test, including its components, price, sample condition, report delivery, method, test type, doctor, test department, and pre-test information.

Test Details

The KCNH1 gene is associated with Temple-Baraitser syndrome, a rare genetic disorder characterized by intellectual disability, epilepsy, distinctive facial features, and developmental delay. The NGS genetic test refers to Next-Generation Sequencing, a technology used to analyze the DNA sequence of a person’s genes.

Components and Price

The KCNH1 Gene Temple-Baraitser syndrome Genetic Test costs 4400.0 AED. The test requires a blood sample, extracted DNA, or one drop of blood on an FTA Card.

Report Delivery

The report for the KCNH1 Gene Temple-Baraitser syndrome Genetic Test is typically delivered within 3 to 4 weeks.

Method

The test utilizes NGS technology to analyze the entire KCNH1 gene for any variations or mutations that may be present.

Test Type

The KCNH1 Gene Temple-Baraitser syndrome Genetic Test falls under the category of dysmorphology.

Doctor and Test Department

The test is conducted by our expert pediatricians in the Genetics department.

Pre Test Information

Prior to undergoing the KCNH1 Gene Temple-Baraitser syndrome Genetic Test, it is essential to provide the clinical history of the patient. Additionally, a genetic counseling session is conducted to draw a pedigree chart of family members affected by KCNH1 Gene Temple-Baraitser syndrome.

Interpreting the Results

It is important to note that the NGS genetic test for Temple-Baraitser syndrome should be interpreted by a healthcare professional with expertise in genetics. The results can help confirm a diagnosis of Temple-Baraitser syndrome and provide information about the specific genetic mutation causing the condition. This information is crucial for genetic counseling and family planning decisions.

Conclusion

The KCNH1 Gene Temple-Baraitser syndrome Genetic Test offered by DNA Labs UAE is a valuable tool for diagnosing Temple-Baraitser syndrome and providing essential genetic counseling to affected individuals and their families. By identifying the specific KCNH1 gene mutation, the NGS test helps in understanding the inheritance pattern and recurrence risk. For accurate interpretation of the results, it is recommended to consult a healthcare professional with expertise in genetics.

Test Name KCNH1 Gene Temple-Baraitser 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 KCNH1 Gene Temple-Baraitser syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with KCNH1 Gene Temple-Baraitser syndrome NGS Genetic DNA Test gene KCNH1
Test Details

The KCNH1 gene is associated with Temple-Baraitser syndrome, a rare genetic disorder characterized by intellectual disability, epilepsy, distinctive facial features, and developmental delay. The NGS genetic test refers to Next-Generation Sequencing, a technology used to analyze the DNA sequence of a person’s genes.

The NGS genetic test for KCNH1 gene mutations involves sequencing the entire gene to identify any variations or mutations that may be present. This test can help in confirming a diagnosis of Temple-Baraitser syndrome and provide information about the specific genetic mutation causing the condition.

By identifying the specific KCNH1 gene mutation, the NGS test can also help in providing information about the inheritance pattern and recurrence risk for affected individuals and their families. This can be important for genetic counseling and family planning decisions.

It is important to note that the NGS genetic test for Temple-Baraitser syndrome is typically performed by a geneticist or genetic counselor, and the results should be interpreted by a healthcare professional with expertise in genetics.

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