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LPIN1 Gene Myoglobinuria Acute Recurrent Genetic Test Cost

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

-21%

The LPIN1 gene plays a crucial role in lipid metabolism within the body. Mutations in this gene can lead to a condition known as acute recurrent myoglobinuria, which is characterized by repeated episodes of muscle pain, weakness, and the release of myoglobin into the urine. This condition can lead to serious complications, including kidney damage, if not diagnosed and managed properly.

DNA Labs UAE offers a genetic test specifically designed to identify mutations in the LPIN1 gene that are associated with acute recurrent myoglobinuria. This test is crucial for individuals who have experienced symptoms of the condition or have a family history of similar symptoms. Early detection through this genetic test can facilitate timely management and intervention strategies to prevent complications.

The cost of the LPIN1 Gene Myoglobinuria Acute Recurrent Genetic Test at DNA Labs UAE is 4400 AED. This test is a valuable tool for healthcare providers in diagnosing this rare but potentially severe condition, allowing for personalized treatment plans based on the genetic makeup of the individual.

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LPIN1 Gene Myoglobinuria Acute Recurrent Genetic Test

Welcome to DNA Labs UAE, where we offer the LPIN1 Gene Myoglobinuria Acute Recurrent Genetic Test. This test helps diagnose myoglobinuria, a condition characterized by recurrent episodes of muscle pain, weakness, and dark urine.

Test Details

The LPIN1 gene is associated with myoglobinuria and plays a role in lipid metabolism. Our Next-Generation Sequencing (NGS) technology allows for a comprehensive analysis of the genetic information, providing a more accurate diagnosis and potentially guiding treatment decisions.

Components and Price

The LPIN1 Gene Myoglobinuria Acute Recurrent Genetic Test costs 4400.0 AED. The test can be conducted using blood or extracted DNA, or even one drop of blood on an FTA card.

Sample Condition

The sample condition required for this test is blood or extracted DNA. Alternatively, one drop of blood can be collected on an FTA card.

Report Delivery

The report for this test is typically delivered within 3 to 4 weeks.

Test Type and Department

The LPIN1 Gene Myoglobinuria Acute Recurrent Genetic Test falls under the category of Neurological Disorders. It is conducted by our Genetics department.

Pre Test Information

Prior to the test, we recommend providing the clinical history of the patient who is going for the LPIN1 Gene Myoglobinuria Acute Recurrent NGS Genetic DNA Test. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected by LPIN1 Gene Myoglobinuria Acute Recurrent.

Doctor and Method

The LPIN1 Gene Myoglobinuria Acute Recurrent Genetic Test is conducted by a Neurologist using NGS Technology.

Benefits and Usage

NGS genetic testing for myoglobinuria can help confirm the diagnosis, identify the specific LPIN1 gene mutation, and provide valuable information for genetic counseling and family planning. It can also aid in predicting the prognosis and guiding treatment options for individuals with myoglobinuria.

Test Name LPIN1 Gene Myoglobinuria acute recurrent 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 LPIN1 Gene Myoglobinuria acute recurrent NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with LPIN1 Gene Myoglobinuria acute recurrent
Test Details

The LPIN1 gene is associated with myoglobinuria, a condition characterized by recurrent episodes of muscle pain, weakness, and dark urine. LPIN1 gene mutations can lead to a deficiency in the enzyme lipin-1, which plays a role in lipid metabolism.

NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously. In the context of myoglobinuria, NGS genetic testing can identify mutations in the LPIN1 gene that may be responsible for the condition. This type of testing allows for a comprehensive analysis of the genetic information, providing a more accurate diagnosis and potentially guiding treatment decisions.

NGS genetic testing for myoglobinuria can help confirm the diagnosis, identify the specific LPIN1 gene mutation, and provide valuable information for genetic counseling and family planning. It can also aid in predicting the prognosis and guiding treatment options for individuals with myoglobinuria.

SKU: TEST-1787 Category:

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