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LTBP2 Gene Weill-Marchesani Syndrome Type 3 Genetic Test Cost

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

-21%

The LTBP2 Gene Weill-Marchesani Syndrome Type 3 Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to detect mutations in the LTBP2 gene, which are associated with Weill-Marchesani Syndrome Type 3 (WMS3). Weill-Marchesani Syndrome is a rare genetic disorder characterized by short stature, reduced joint flexibility, and eye abnormalities, among other symptoms. The LTBP2 gene plays a crucial role in the development and maintenance of the body’s connective tissue, and mutations in this gene can lead to the manifestations of WMS3.

This genetic test is vital for individuals with a clinical diagnosis suggestive of Weill-Marchesani Syndrome or for those with a family history of the condition, as it can provide definitive genetic evidence of WMS3. Early diagnosis through genetic testing can significantly impact the management and treatment of the syndrome, allowing for personalized care plans and interventions to improve the quality of life for affected individuals.

The test is conducted at DNA Labs UAE, a reputable facility known for its advanced genetic testing services. The cost of the LTBP2 Gene Weill-Marchesani Syndrome Type 3 Genetic Test is 4400 AED. This investment covers the genetic analysis and the comprehensive report that details the findings, providing a clear understanding of the individual’s genetic status concerning the LTBP2 gene mutations.

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LTBP2 Gene Weill-Marchesani syndrome type 3 Genetic Test

At DNA Labs UAE, we offer the LTBP2 Gene Weill-Marchesani syndrome type 3 Genetic Test at a cost of AED 4400.0.

Test Details

The LTBP2 gene is associated with Weill-Marchesani syndrome type 3, a rare genetic disorder characterized by short stature, joint stiffness, and eye abnormalities.

NGS (Next-Generation Sequencing) Genetic Test refers to a type of genetic testing that uses high-throughput sequencing technologies to analyze multiple genes simultaneously. In the case of Weill-Marchesani syndrome type 3, NGS can be used to sequence the LTBP2 gene and identify any genetic variations or mutations that may be responsible for the condition.

By performing an NGS Genetic Test for the LTBP2 gene, healthcare professionals can diagnose Weill-Marchesani syndrome type 3 and provide appropriate medical management and genetic counseling for affected individuals and their families.

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 the LTBP2 Gene Weill-Marchesani syndrome type 3 NGS Genetic DNA Test, it is important 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 with the LTBP2 Gene Weill-Marchesani syndrome type 3 NGS Genetic DNA Test gene LTBP2.

Genetic counselling is essential in order to understand the inheritance pattern of the condition and to provide appropriate guidance and support to affected individuals and their families.

For more information or to schedule an appointment, please contact DNA Labs UAE.

Test Name LTBP2 Gene Weill-Marchesani 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 Dysmorphology
Doctor Pediatrics
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for LTBP2 Gene Weill-Marchesani syndrome type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with LTBP2 Gene Weill-Marchesani syndrome type 3 NGS Genetic DNA Test gene LTBP2
Test Details

The LTBP2 gene is associated with Weill-Marchesani syndrome type 3, a rare genetic disorder characterized by short stature, joint stiffness, and eye abnormalities.

NGS (Next-Generation Sequencing) Genetic Test refers to a type of genetic testing that uses high-throughput sequencing technologies to analyze multiple genes simultaneously. In the case of Weill-Marchesani syndrome type 3, NGS can be used to sequence the LTBP2 gene and identify any genetic variations or mutations that may be responsible for the condition.

By performing an NGS Genetic Test for the LTBP2 gene, healthcare professionals can diagnose Weill-Marchesani syndrome type 3 and provide appropriate medical management and genetic counseling for affected individuals and their families.

SKU: TEST-4438 Category:

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