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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 myoglobinuria acute recurrent genetic test is a specialized diagnostic tool designed to identify mutations in the LPIN1 gene, which are associated with acute recurrent myoglobinuria. Myoglobinuria is a condition characterized by the presence of myoglobin in the urine, typically resulting from muscle damage. When the LPIN1 gene is mutated, it can lead to episodes of rhabdomyolysis, where muscle fibers break down rapidly, releasing myoglobin into the bloodstream, and subsequently, the urine. This condition can cause acute kidney injury and other serious health issues.

DNA Labs UAE offers this genetic test at a cost of 4400 AED. The test involves analyzing the patient’s DNA to detect any genetic alterations in the LPIN1 gene that might predispose them to episodes of acute recurrent myoglobinuria. This test is crucial for individuals who have experienced unexplained episodes of muscle pain, weakness, or dark-colored urine, as it can help in the diagnosis and management of the condition. Early identification of the genetic mutation can lead to better management strategies, including lifestyle adjustments and medical interventions to prevent or minimize the impact of rhabdomyolysis episodes.

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LPIN1 Gene Myoglobinuria Acute Recurrent Genetic Test

At DNA Labs UAE, we offer the LPIN1 Gene Myoglobinuria Acute Recurrent Genetic Test for the diagnosis of myoglobinuria acute recurrent. This genetic test helps in identifying specific genetic variations in the LPIN1 gene that may be causing the condition.

Test Details

The LPIN1 gene is associated with myoglobinuria acute recurrent, a condition characterized by recurrent episodes of muscle pain, weakness, and myoglobinuria. These episodes can be triggered by exercise, fasting, or infections.

Components and Price

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

Report Delivery

After the test is conducted, the report will be delivered within 3 to 4 weeks.

Method

The LPIN1 Gene Myoglobinuria Acute Recurrent Genetic Test is performed using NGS (Next-Generation Sequencing) technology. This technology allows for the simultaneous analysis of multiple genes, including the LPIN1 gene.

Test Type

The LPIN1 Gene Myoglobinuria Acute Recurrent Genetic Test falls under the category of Vascular Diseases.

Doctor and Test Department

This test is conducted by our team of General Physicians in the Genetics department.

Pre Test Information

Prior to conducting the LPIN1 Gene Myoglobinuria Acute Recurrent Genetic Test, it is important to gather the clinical history of the patient. Additionally, a genetic counseling session is recommended to draw a pedigree chart of family members affected by the LPIN1 gene.

Benefits of the Test

By performing the LPIN1 Gene Myoglobinuria Acute Recurrent Genetic Test, healthcare professionals can identify specific genetic variations that may be causing myoglobinuria acute recurrent. This information can aid in the diagnosis, prognosis, and management of the condition. It can also be useful for genetic counseling and family planning purposes.

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
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Vascular Diseases
Doctor General Physician
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 NGS Genetic DNA Test gene LPIN1
Test Details

The LPIN1 gene is associated with a condition called myoglobinuria acute recurrent. Myoglobinuria refers to the presence of myoglobin in the urine, which is a protein found in muscle tissues. This condition is characterized by recurrent episodes of muscle pain, weakness, and myoglobinuria, which can be triggered by exercise, fasting, or infections.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes, including the LPIN1 gene. NGS technology enables the sequencing of the entire coding region of a gene, providing a comprehensive analysis of genetic variations that may be contributing to the disease.

By performing an NGS genetic test for LPIN1 gene mutations, healthcare professionals can identify specific genetic variations that may be causing myoglobinuria acute recurrent. This information can help with the diagnosis, prognosis, and management of the condition. It may also be useful for genetic counseling and family planning purposes.

SKU: TEST-3538 Category:

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