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FKRP Gene Muscular Dystrophy Type 1C Genetic Test Cost

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

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The FKRP gene muscular dystrophy type 1C genetic test is a specialized diagnostic procedure aimed at identifying mutations in the FKRP gene, which are known to cause a form of limb-girdle muscular dystrophy (LGMD1C). This condition is characterized by progressive weakness and wasting of the muscles around the hips and shoulders, affecting mobility and physical capabilities over time. The test involves analyzing the patient’s DNA to pinpoint any genetic abnormalities in the FKRP gene, which plays a crucial role in muscle function and integrity.

Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the test is priced at 4400 AED. This cost encompasses the full process of sample collection, genetic sequencing, and expert analysis to ensure accurate identification of any mutations associated with the condition. The results from this test are critical for confirming a diagnosis of LGMD1C, which can then guide treatment options and genetic counseling for affected individuals and their families. This genetic test is a key step towards personalized care, offering insights into the specific genetic alterations driving the disease and enabling targeted management strategies.

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FKRP Gene Muscular Dystrophy Type 1C Genetic Test

At DNA Labs UAE, we offer the FKRP Gene Muscular Dystrophy Type 1C Genetic Test. This test is used to diagnose or confirm the diagnosis of muscular dystrophy type 1C, a rare form of muscular dystrophy caused by mutations in the FKRP gene.

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: Neurological Disorders
  • Doctor: Neurologist
  • Test Department: Genetics

Pre Test Information

Prior to undergoing the FKRP Gene Muscular Dystrophy Type 1C Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected with FKRP Gene Muscular Dystrophy Type 1C.

Test Details

The FKRP Gene Muscular Dystrophy Type 1C Genetic Test utilizes NGS (Next Generation Sequencing) technology to analyze the FKRP gene for mutations or variations. This comprehensive sequencing allows for the detection of various types of mutations, including small insertions, deletions, or single nucleotide changes.

By identifying mutations in the FKRP gene, this test can help determine the underlying cause of the muscular dystrophy and provide valuable information for genetic counseling and management of the condition. It is important to note that this test specifically focuses on muscular dystrophy type 1C caused by mutations in the FKRP gene and may not detect mutations in other genes associated with different types of muscular dystrophy.

Please keep in mind that while this test is highly accurate, it may not detect all possible mutations in the FKRP gene. There could be variations that are not yet known or included in the test panel. Therefore, a negative test result does not completely rule out the possibility of having muscular dystrophy type 1C.

Test Name FKRP Gene Muscular dystrophy type 1C 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 FKRP Gene Muscular dystrophy type 1C NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with FKRP Gene Muscular dystrophy type 1C
Test Details

FKRP gene muscular dystrophy type 1C NGS genetic test is a genetic test that analyzes the FKRP gene for mutations or variations. This test is used to diagnose or confirm the diagnosis of muscular dystrophy type 1C, which is a rare form of muscular dystrophy caused by mutations in the FKRP gene.

NGS (Next Generation Sequencing) technology is used in this test to sequence the entire FKRP gene, allowing for the detection of various types of mutations, including small insertions, deletions, or single nucleotide changes. By identifying mutations in the FKRP gene, this test can help determine the underlying cause of the muscular dystrophy and provide information for genetic counseling and management of the condition.

It is important to note that this test specifically focuses on muscular dystrophy type 1C caused by mutations in the FKRP gene and may not detect mutations in other genes associated with different types of muscular dystrophy. Additionally, this test may not detect all possible mutations in the FKRP gene, as there could be variations that are not yet known or included in the test panel. Therefore, a negative test result does not completely rule out the possibility of having muscular dystrophy type 1C.

SKU: TEST-1747 Category:

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