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TMEM38B Gene Osteogenesis Imperfecta Type 14 Genetic Test Cost

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

-21%

The TMEM38B Gene Osteogenesis Imperfecta Type 14 Genetic Test is a specialized diagnostic tool designed to identify mutations in the TMEM38B gene, which are linked to Osteogenesis Imperfecta (OI) Type 14. Osteogenesis Imperfecta, also known as brittle bone disease, is a group of genetic disorders that mainly affect the bones, leading to their increased fragility and susceptibility to fractures. Type 14 of this condition is a rare form attributed to specific genetic anomalies in the TMEM38B gene.

This genetic test involves analyzing the patient’s DNA to search for mutations in the TMEM38B gene that are known to cause the disease. Identifying these mutations can confirm a diagnosis of OI Type 14, allowing for appropriate management and treatment plans to be developed. It can also provide essential information for family planning and genetic counseling for affected families.

The test is available at DNA Labs UAE, a leading provider of genetic testing services in the United Arab Emirates. DNA Labs UAE employs state-of-the-art technology and methodologies to ensure accurate and reliable results. The cost of the TMEM38B Gene Osteogenesis Imperfecta Type 14 Genetic Test is 4400 AED, reflecting the specialized nature of the test and the expertise required to interpret its results.

By opting for this test, patients and their families can gain valuable insights into their genetic health, enabling informed decisions about their medical care and future.

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  • 100% accuaret Test Results
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  • This test is not intended for medical diagnosis or treatment
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TMEM38B Gene Osteogenesis imperfecta type 14 Genetic Test

At DNA Labs UAE, we offer the TMEM38B Gene Osteogenesis imperfecta type 14 Genetic Test at a cost of AED 4400.0.

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

Prior to undergoing the TMEM38B Gene Osteogenesis imperfecta type 14 Genetic 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 TMEM38B Gene Osteogenesis imperfecta type 14 NGS Genetic DNA Test gene TMEM38B.

Test Details

The TMEM38B gene is associated with Osteogenesis Imperfecta type 14 (OI type 14), which is a group of genetic disorders characterized by fragile bones and susceptibility to fractures. OI type 14 is caused by mutations in the TMEM38B gene, which is involved in the regulation of calcium transport in cells.

NGS (Next-Generation Sequencing) Genetic Testing is a method used to analyze multiple genes simultaneously for mutations or variations. In the context of OI type 14, NGS Genetic Testing can be used to identify mutations in the TMEM38B gene that are responsible for the condition.

This test can help in confirming a diagnosis, providing genetic counseling, and guiding treatment options for individuals suspected of having OI type 14. NGS Genetic Testing involves sequencing the DNA of the individual being tested, typically using a blood or saliva sample. The DNA is then analyzed using advanced sequencing technologies to identify any mutations or variations in the TMEM38B gene.

The results of the test can help healthcare professionals understand the underlying genetic cause of OI type 14 in an individual and provide personalized care. It is important to note that genetic testing should be performed by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate guidance and support.

Test Name TMEM38B Gene Osteogenesis imperfecta type 14 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 TMEM38B Gene Osteogenesis imperfecta type 14 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TMEM38B Gene Osteogenesis imperfecta type 14 NGS Genetic DNA Test gene TMEM38B
Test Details

The TMEM38B gene is associated with Osteogenesis Imperfecta type 14 (OI type 14). Osteogenesis Imperfecta is a group of genetic disorders characterized by fragile bones and susceptibility to fractures. OI type 14 is caused by mutations in the TMEM38B gene, which is involved in the regulation of calcium transport in cells.

NGS (Next-Generation Sequencing) Genetic Testing is a method used to analyze multiple genes simultaneously for mutations or variations. In the context of OI type 14, NGS Genetic Testing can be used to identify mutations in the TMEM38B gene that are responsible for the condition. This test can help in confirming a diagnosis, providing genetic counseling, and guiding treatment options for individuals suspected of having OI type 14.

NGS Genetic Testing involves sequencing the DNA of the individual being tested, typically using a blood or saliva sample. The DNA is then analyzed using advanced sequencing technologies to identify any mutations or variations in the TMEM38B gene. The results of the test can help healthcare professionals understand the underlying genetic cause of OI type 14 in an individual and provide personalized care.

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

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