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MNX1 Gene Currarino Syndrome Genetic Test Cost

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

-21%

The MNX1 gene plays a critical role in human development, and mutations in this gene are associated with Currarino Syndrome, a rare congenital disorder characterized by a triad of anomalies: a presacral mass (like a teratoma or anterior meningocele), anorectal malformations, and sacral bone deformity. Currarino Syndrome is inherited in an autosomal dominant pattern, meaning a single copy of the altered gene in each cell is sufficient to cause the disorder.

Recognizing the importance of accurate diagnosis for effective management and treatment, DNA Labs UAE offers a genetic test specifically designed to detect mutations in the MNX1 gene associated with Currarino Syndrome. This test is a crucial tool for clinicians in diagnosing the syndrome, enabling them to provide tailored treatment plans for affected individuals. It involves collecting a DNA sample, typically through a blood draw or cheek swab, and analyzing the genetic material for specific mutations in the MNX1 gene.

The cost of the MNX1 gene Currarino Syndrome genetic test at DNA Labs UAE is 4400 AED. This price reflects the comprehensive analysis and the personalized care and consultation that accompany the testing process. Given the specialized nature of this test, it is a valuable investment for families seeking answers to complex genetic questions related to Currarino Syndrome.

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MNX1 Gene Currarino Syndrome Genetic Test

Are you concerned about Currarino syndrome? DNA Labs UAE offers the MNX1 Gene Currarino Syndrome Genetic Test at an affordable price of AED 4400.0. This comprehensive test can help diagnose Currarino syndrome and provide valuable insights into the specific genetic changes associated with this rare genetic disorder.

Test Components and Price

  • Test Name: MNX1 Gene Currarino Syndrome Genetic Test
  • Components: Blood or Extracted DNA or One drop Blood on FTA Card
  • Price: 4400.0 AED

Report Delivery and Method

With our state-of-the-art NGS (Next-Generation Sequencing) technology, we can deliver accurate and reliable results within 3 to 4 weeks. This advanced sequencing method allows us to analyze multiple genes simultaneously, including the MNX1 gene associated with Currarino syndrome.

Test Type and Doctor

Our MNX1 Gene Currarino Syndrome Genetic Test falls under the Dysmorphology test type. It is recommended to consult with a qualified Pediatrics doctor who specializes in genetics for this test.

Test Department and Pre-Test Information

Our Genetics department handles the MNX1 Gene Currarino Syndrome Genetic Test. Before undergoing the test, it is essential to provide the clinical history of the patient. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected by Currarino syndrome.

About Currarino Syndrome and the MNX1 Gene

Currarino syndrome is a rare genetic disorder characterized by abnormalities in the lower spine, anus, and rectum. Individuals with this syndrome may have anorectal malformations, such as abnormal connections between the rectum and urinary tract or the rectum and vagina. Malformations in the sacrum, the base of the spine, are also common.

The MNX1 gene is associated with Currarino syndrome. Our NGS genetic testing can identify mutations or variations in the MNX1 gene, helping in the diagnosis of Currarino syndrome and providing valuable information about the specific genetic changes present in an individual.

It is important to note that genetic testing for Currarino syndrome should only be performed by a qualified healthcare professional or genetic counselor. They can interpret the test results and provide appropriate counseling and support based on the findings.

Don’t delay in getting the MNX1 Gene Currarino Syndrome Genetic Test at DNA Labs UAE. Our affordable price and accurate results can help you understand and manage Currarino syndrome better.

Test Name MNX1 Gene Currarino 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 MNX1 Gene Currarino syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MNX1 Gene Currarino syndrome NGS Genetic DNA Test gene MNX1
Test Details

The MNX1 gene is associated with a condition called Currarino syndrome. Currarino syndrome is a rare genetic disorder characterized by the presence of certain abnormalities in the lower spine, anus, and rectum. Individuals with Currarino syndrome may have anorectal malformations, such as an abnormal connection between the rectum and urinary tract or the rectum and vagina, as well as malformations in the sacrum (the base of the spine).

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of Currarino syndrome, NGS genetic testing can be used to identify mutations or variations in the MNX1 gene that are associated with the condition. This type of genetic testing can help in the diagnosis of Currarino syndrome and provide information about the specific genetic changes present in an individual.

It is important to note that genetic testing for Currarino syndrome should be performed by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate counseling and support.