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KBTBD13 Gene Nemaline Myopathy Type 6 Genetic Test Cost

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

-21%

The KBTBD13 Gene Nemaline Myopathy Type 6 Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to identify mutations in the KBTBD13 gene, which are responsible for causing Nemaline Myopathy Type 6. This rare genetic disorder is characterized by muscle weakness, hypotonia, and the presence of rod-like structures in muscle cells, known as nemaline bodies. Early diagnosis through this genetic test is crucial for managing symptoms and improving the quality of life for affected individuals. The test is priced at 4400 AED and is conducted in the advanced facilities of DNA Labs UAE, ensuring accurate and reliable results. By analyzing a small sample of the patient’s DNA, this test provides valuable information for genetic counseling and guides decision-making regarding treatment options.

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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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KBTBD13 Gene Nemaline Myopathy Type 6 Genetic Test

Welcome to DNA Labs UAE, where we offer the KBTBD13 Gene Nemaline Myopathy Type 6 Genetic Test. This test is designed to diagnose and provide information about the cost, symptoms, and diagnosis of Nemaline Myopathy Type 6.

Test Details

The KBTBD13 gene is associated with Nemaline Myopathy Type 6, a rare genetic muscle disorder characterized by muscle weakness and low muscle tone (hypotonia). Our Next-Generation Sequencing (NGS) technology allows for the simultaneous analysis of multiple genes, including the KBTBD13 gene.

Test Components and Price

  • Test Name: KBTBD13 Gene Nemaline Myopathy Type 6 Genetic Test
  • Components: NGS Technology
  • Price: 4400.0 AED

Sample Condition

We require a blood or extracted DNA sample for this test. Alternatively, one drop of blood on an FTA Card can also be used.

Report Delivery

You can expect to receive your test results within 3 to 4 weeks after sample submission.

Test Type and Doctor

This test falls under the category of Neurological Disorders and is performed by our experienced Neurologist. Our dedicated Test Department specializing in Genetics will handle your case.

Pre Test Information

Prior to the test, we recommend providing the clinical history of the patient who is undergoing the KBTBD13 Gene Nemaline Myopathy Type 6 NGS Genetic DNA Test. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected by this condition.

Understanding the Test

NGS genetic testing involves obtaining a DNA sample, typically through a blood or saliva sample. The DNA is then sequenced to analyze the specific genes of interest, including the KBTBD13 gene. The test results can help confirm a diagnosis, understand the underlying cause of the condition, and provide valuable information for treatment and management options.

At DNA Labs UAE, we strive to provide accurate and reliable genetic testing services. If you suspect Nemaline Myopathy Type 6 or have any concerns about your genetic health, we encourage you to consult with our team of experts.

Test Name KBTBD13 Gene Nemaline myopathy type 6 Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card o
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Neurological Disorders
Doctor Neurologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for KBTBD13 Gene Nemaline myopathy type 6 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with KBTBD13 Gene Nemaline myopathy type 6
Test Details

The KBTBD13 gene is associated with nemaline myopathy type 6, which is a rare genetic muscle disorder characterized by muscle weakness and hypotonia (low muscle tone).

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes, including the KBTBD13 gene. This test can identify any genetic variations or mutations in the KBTBD13 gene that may be causing or contributing to nemaline myopathy type 6.

NGS genetic testing involves obtaining a DNA sample, usually through a blood or saliva sample, and then sequencing the DNA to analyze the specific genes of interest. The results of the test can help in confirming a diagnosis, understanding the underlying cause of the condition, and informing treatment and management options.