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TMEM67 Gene Meckel Syndrome Type 3 Genetic Test

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

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The TMEM67 gene plays a crucial role in the development and function of primary cilia, which are microscopic cellular structures involved in signal transduction and cellular growth. Mutations in the TMEM67 gene are associated with Meckel syndrome type 3 (MKS3), a rare genetic disorder characterized by kidney cysts, liver fibrosis, and neurological anomalies, among other symptoms. Given the severity and complexity of MKS3, early and accurate diagnosis is vital for managing the condition.

The TMEM67 Gene Meckel Syndrome Type 3 Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to detect mutations in the TMEM67 gene that are indicative of MKS3. This test is critical for families with a history of MKS3, as it can provide essential information for genetic counseling, prenatal diagnosis, and personalized management plans for affected individuals.

The cost of the test is 4400 AED, reflecting the comprehensive analysis and the sophisticated technology employed to ensure accurate results. Conducted in the state-of-the-art facilities of DNA Labs UAE, the test adheres to the highest standards of genetic testing, providing reliable and timely information for affected families.

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  • This test is not intended for medical diagnosis or treatment
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TMEM67 Gene Meckel Syndrome Type 3 Genetic Test

Welcome to DNA Labs UAE, where we offer the TMEM67 Gene Meckel syndrome type 3 Genetic Test. This blog will provide you with detailed information about the test, including its components, price, sample condition, report delivery, method, test type, doctor, test department, pre-test information, and test details.

Test Components

  • Test Name: TMEM67 Gene Meckel syndrome type 3 Genetic Test
  • Price: 4400.0 AED

Sample Condition

The test requires one of the following sample conditions:

  • Blood
  • Extracted DNA
  • One drop of blood on FTA Card

Report Delivery

The report will be delivered within 3 to 4 weeks.

Method

The test utilizes NGS (Next-Generation Sequencing) technology.

Test Type

The test is focused on Hepatology, Nephrology, and Endocrinology Disorders.

Doctor

The test is conducted by a General Physician.

Test Department

The test is performed in our Genetics department.

Pre Test Information

Prior to the test, it is important to provide the clinical history of the patient who is undergoing the TMEM67 Gene Meckel syndrome type 3 NGS Genetic DNA Test. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected by TMEM67 Gene Meckel syndrome type 3 NGS Genetic DNA Test gene TMEM67.

Test Details

The TMEM67 gene is associated with Meckel syndrome type 3, also known as MKS3. Meckel syndrome is a rare genetic disorder characterized by developmental abnormalities affecting multiple organs. MKS3 is one of the subtypes of Meckel syndrome, and it is caused by mutations in the TMEM67 gene.

NGS (Next-Generation Sequencing) genetic testing is a highly efficient and cost-effective method for identifying genetic mutations associated with various disorders, including Meckel syndrome type 3. This type of genetic test allows for the simultaneous analysis of multiple genes or even the entire genome.

By performing an NGS genetic test on the TMEM67 gene, healthcare professionals can identify any mutations or variations in this gene that may be causing or contributing to the development of Meckel syndrome type 3. This information can be used for accurate diagnosis, genetic counseling, and potentially targeted treatment or management strategies for individuals affected by this disorder.

Test Name TMEM67 Gene Meckel syndrome type 3 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 Hepatology Nephrology Endocrinology Disorders
Doctor General Physician
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for TMEM67 Gene Meckel syndrome type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TMEM67 Gene Meckel syndrome type 3 NGS Genetic DNA Test gene TMEM67
Test Details

The TMEM67 gene is associated with Meckel syndrome type 3, also known as MKS3. Meckel syndrome is a rare genetic disorder characterized by developmental abnormalities affecting multiple organs. MKS3 is one of the subtypes of Meckel syndrome, and it is caused by mutations in the TMEM67 gene.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that allows for the simultaneous analysis of multiple genes or even the entire genome. It is a highly efficient and cost-effective method for identifying genetic mutations associated with various disorders, including Meckel syndrome type 3.

By performing an NGS genetic test on the TMEM67 gene, healthcare professionals can identify any mutations or variations in this gene that may be causing or contributing to the development of Meckel syndrome type 3. This information can be used for accurate diagnosis, genetic counseling, and potentially targeted treatment or management strategies for individuals affected by this disorder.

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