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SOST Gene Sclerosteosis Type 1 Genetic Test Cost

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

-21%

The SOST Gene Sclerosteosis Type 1 Genetic Test is a specialized diagnostic tool used to identify mutations in the SOST gene, which are responsible for causing Sclerosteosis Type 1, a rare genetic disorder. This condition is characterized by excessive bone growth that can lead to various complications, including facial distortion, entrapment of cranial nerves, and increased intracranial pressure. Early and accurate diagnosis through this genetic test enables appropriate management and treatment strategies for affected individuals.

The test is conducted at DNA Labs UAE, a leading facility in genetic testing and diagnostics. The cost of the test is set at 4400 AED. DNA Labs UAE utilizes advanced genomic technologies to ensure high accuracy and reliability of the test results, providing essential information for patients and healthcare providers in managing Sclerosteosis Type 1 effectively.

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SOST Gene Sclerosteosis Type 1 Genetic Test

At DNA Labs UAE, we offer the SOST Gene Sclerosteosis Type 1 Genetic Test at a cost of AED 4400.0. This test is used to diagnose sclerosteosis type 1, a rare genetic disorder characterized by abnormal bone growth and increased bone density.

Test Details

The SOST gene sclerosteosis type 1 NGS genetic test utilizes Next Generation Sequencing (NGS) technology to analyze the SOST gene for mutations associated with the condition. The SOST gene encodes a protein called sclerostin, which normally inhibits bone formation. Mutations in the SOST gene lead to excessive bone growth.

This diagnostic test involves sequencing the entire coding region of the SOST gene to identify any changes or mutations. It can detect both small point mutations and larger deletions or insertions in the gene.

The test is typically performed on a blood or saliva sample from the individual suspected of having sclerosteosis type 1. The DNA is extracted from the sample and then sequenced using NGS technology. The resulting sequence data is analyzed to identify any mutations or variants in the SOST gene.

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 SOST Gene Sclerosteosis Type 1 NGS Genetic DNA Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by sclerosteosis type 1.

Uses of the Test

The SOST gene sclerosteosis type 1 NGS genetic test can confirm a diagnosis of sclerosteosis type 1 in individuals with clinical symptoms. It can also be used for carrier testing in individuals with a family history of the condition. Furthermore, it can be utilized for prenatal testing in families with a known SOST gene mutation.

It is important to note that this test specifically targets mutations in the SOST gene associated with sclerosteosis type 1 and does not analyze other genes or conditions.

Genetic Counseling

Both before and after undergoing the SOST gene sclerosteosis type 1 NGS genetic test, it is recommended to seek genetic counseling. This allows for a discussion of the implications of the test results and any potential treatment options.

Test Name SOST Gene Sclerosteosis type 1 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 SOST Gene Sclerosteosis type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SOST Gene Sclerosteosis type 1 NGS Genetic DNA Test gene SOST
Test Details

SOST gene sclerosteosis type 1 NGS genetic test is a diagnostic test that uses Next Generation Sequencing (NGS) technology to analyze the SOST gene for mutations associated with sclerosteosis type 1.

Sclerosteosis type 1 is a rare genetic disorder characterized by abnormal bone growth and increased bone density. It is caused by mutations in the SOST gene, which encodes a protein called sclerostin. Sclerostin normally inhibits bone formation, so mutations in the SOST gene lead to excessive bone growth.

The NGS genetic test for SOST gene mutations involves sequencing the entire coding region of the gene to identify any changes or mutations. This test can detect both small point mutations as well as larger deletions or insertions in the gene.

The test is typically performed on a blood or saliva sample from the individual suspected of having sclerosteosis type 1. The DNA is extracted from the sample and then sequenced using NGS technology. The resulting sequence data is analyzed to identify any mutations or variants in the SOST gene.

The SOST gene sclerosteosis type 1 NGS genetic test can confirm a diagnosis of sclerosteosis type 1 in individuals with clinical symptoms and can also be used for carrier testing in individuals with a family history of the condition. It can also be used for prenatal testing in families with a known SOST gene mutation.

It is important to note that this test specifically targets mutations in the SOST gene associated with sclerosteosis type 1 and does not analyze other genes or conditions. Genetic counseling is typically recommended both before and after undergoing this test to discuss the implications of the results and any potential treatment options.