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TNXB Gene Ehlers-Danlos Syndrome Type 3 Genetic Test Cost

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

-21%

The TNXB Gene Ehlers-Danlos Syndrome Type 3 Genetic Test is a specialized diagnostic procedure aimed at identifying mutations in the TNXB gene, which are associated with Ehlers-Danlos Syndrome Type 3, also known as Hypermobility Type. This condition is characterized by symptoms including joint hypermobility, skin hyperextensibility, and tissue fragility. The test involves collecting a DNA sample, typically through a blood draw or cheek swab, and analyzing the genetic material for specific mutations in the TNXB gene that are linked to this syndrome.

Performed at DNA Labs UAE, a leading facility in genetic testing and analysis, the test offers individuals and families critical insights into their genetic predispositions and aids in the management and treatment of Ehlers-Danlos Syndrome Type 3. The cost of the test is 4400 AED, reflecting the comprehensive nature of the analysis and the expertise required to interpret the results accurately. This genetic test is a valuable tool for those seeking a definitive diagnosis of Ehlers-Danlos Syndrome Type 3, enabling targeted interventions and personalized care plans.

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  • This test is not intended for medical diagnosis or treatment
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TNXB Gene Ehlers-Danlos 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: Osteology Dermatology Immunology Disorders
  • Doctor: Dermatologist
  • Test Department: Genetics

Pre Test Information

Clinical History of Patient who is going for TNXB Gene Ehlers-Danlos syndrome type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TNXB Gene Ehlers-Danlos syndrome type 3 NGS Genetic DNA Test gene TNXB.

Test Details

The TNXB gene is associated with Ehlers-Danlos syndrome (EDS) type 3, also known as hypermobile EDS. EDS is a group of genetic disorders that affect the connective tissues in the body, leading to joint hypermobility, skin elasticity, and other symptoms.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. In the case of TNXB gene testing, NGS can identify specific genetic variations or mutations in the TNXB gene that are associated with EDS type 3.

By performing the TNXB gene NGS genetic test, healthcare professionals can confirm a diagnosis of EDS type 3 in individuals suspected of having the condition. This can help guide treatment decisions and provide important information for patients and their families regarding disease management and genetic counseling.

Test Name TNXB Gene Ehlers-Danlos 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 Osteology Dermatology Immunology Disorders
Doctor Dermatologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for TNXB Gene Ehlers-Danlos syndrome type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TNXB Gene Ehlers-Danlos syndrome type 3 NGS Genetic DNA Test gene TNXB
Test Details

The TNXB gene is associated with Ehlers-Danlos syndrome (EDS) type 3, also known as hypermobile EDS. EDS is a group of genetic disorders that affect the connective tissues in the body, leading to joint hypermobility, skin elasticity, and other symptoms.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. In the case of TNXB gene testing, NGS can identify specific genetic variations or mutations in the TNXB gene that are associated with EDS type 3.

By performing the TNXB gene NGS genetic test, healthcare professionals can confirm a diagnosis of EDS type 3 in individuals suspected of having the condition. This can help guide treatment decisions and provide important information for patients and their families regarding disease management and genetic counseling.