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SLC35D1 Gene Schneckenbecken Dysplasia Genetic Test Cost

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

-21%

The SLC35D1 gene plays a crucial role in the human body, and mutations in this gene are associated with Schneckenbecken dysplasia, a rare and severe skeletal dysplasia characterized by a short trunk, short limbs, and a narrow chest, often leading to perinatal lethality. Given the critical nature of early diagnosis for managing the condition, genetic testing for mutations in the SLC35D1 gene is an essential tool for families at risk.

At DNA Labs UAE, a specialized genetic test is available to identify mutations in the SLC35D1 gene, providing crucial information for expecting parents and individuals with a family history of Schneckenbecken dysplasia. This test, priced at 4400 AED, involves analyzing the individual’s DNA to detect the presence of specific mutations in the SLC35D1 gene that are known to cause the condition. The process is designed to be comprehensive and sensitive, ensuring a high degree of accuracy in the results.

By opting for the SLC35D1 gene Schneckenbecken dysplasia genetic test at DNA Labs UAE, individuals can gain valuable insights into their genetic makeup, enabling them to make informed decisions about their health and future family planning. The test is conducted by a team of skilled professionals who ensure confidentiality and support throughout the testing process, providing a reliable resource for those seeking answers to their genetic questions.

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SLC35D1 Gene Schneckenbecken Dysplasia Genetic Test

At DNA Labs UAE, we offer the SLC35D1 Gene Schneckenbecken Dysplasia Genetic Test at a cost of AED 4400.0. This test is used to diagnose Schneckenbecken dysplasia, a rare genetic disorder that affects the development of bones and joints, particularly in the pelvis and spine.

Test Components

  • Price: AED 4400.0
  • 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

Prior to undergoing the SLC35D1 Gene Schneckenbecken Dysplasia Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected with the SLC35D1 gene. This will help in the analysis and interpretation of the test results.

Test Details

The SLC35D1 gene is specifically associated with Schneckenbecken dysplasia. This genetic disorder is characterized by short stature, abnormal curvature of the spine (scoliosis), and various skeletal abnormalities. Our NGS genetic testing utilizes advanced sequencing technologies to analyze multiple genes simultaneously. In the case of Schneckenbecken dysplasia, NGS can specifically analyze the SLC35D1 gene for any mutations or variants that may be present.

Identifying specific mutations or variants in the SLC35D1 gene through NGS genetic testing can help diagnose individuals with Schneckenbecken dysplasia. This information is valuable for genetic counseling and managing the condition. Additionally, the test can be used for carrier testing in families with a history of the disorder.

It is important to note that genetic testing should always be performed and interpreted by healthcare professionals with expertise in genetics and genetic counseling. They can provide appropriate guidance and support based on the results of the test.

Test Name SLC35D1 Gene Schneckenbecken dysplasia 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 SLC35D1 Gene Schneckenbecken dysplasia NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SLC35D1 Gene Schneckenbecken dysplasia NGS Genetic DNA Test gene SLC35D1
Test Details

The SLC35D1 gene is associated with a rare genetic disorder called Schneckenbecken dysplasia. This disorder affects the development of the bones and joints, particularly in the pelvis and spine. It is characterized by short stature, abnormal curvature of the spine (scoliosis), and various skeletal abnormalities.

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 Schneckenbecken dysplasia, NGS can be used to analyze the SLC35D1 gene for any mutations or variants that may be present.

By identifying specific mutations or variants in the SLC35D1 gene, NGS genetic testing can help diagnose individuals with Schneckenbecken dysplasia and provide valuable information for genetic counseling and management of the condition. It can also be used for carrier testing in families with a history of the disorder.

It’s important to note that genetic testing should be performed and interpreted by healthcare professionals with expertise in genetics and genetic counseling. They can provide appropriate guidance and support based on the results of the test.

SKU: TEST-4353 Category:

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