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PC Gene Pyruvate Carboxylase Deficiency Genetic Test Cost

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

-21%

The PC Gene Pyruvate Carboxylase Deficiency Genetic Test is a specialized diagnostic examination offered by DNA Labs UAE, designed to detect mutations in the PC gene, which are responsible for pyruvate carboxylase deficiency. This condition is a rare metabolic disorder that disrupts the normal processing of carbohydrates and amino acids, leading to a buildup of lactic acid in the body and a range of associated health issues, including developmental delay and neurological problems. The test is critical for early diagnosis and management of the condition, allowing for tailored treatments that can significantly improve the quality of life for affected individuals. The cost of the test is set at 4400 AED, reflecting the comprehensive analysis and expertise required to accurately identify the genetic mutations associated with this disorder.

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PC Gene Pyruvate carboxylase deficiency Genetic Test

Components:

  • Test Name: PC Gene Pyruvate carboxylase deficiency Genetic Test
  • 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: Clinical History of Patient who is going for PC Gene Pyruvate carboxylase deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PC Gene Pyruvate carboxylase deficiency

Test Details:

PC Gene Pyruvate carboxylase deficiency NGS Genetic Test is a genetic test that uses Next-Generation Sequencing (NGS) technology to analyze the PC gene for mutations associated with Pyruvate Carboxylase (PC) deficiency. Pyruvate Carboxylase deficiency is a rare genetic disorder that affects the body’s ability to convert pyruvate into energy. This deficiency can lead to a variety of symptoms, including developmental delays, neurological problems, and metabolic disturbances.

The NGS Genetic Test for PC Gene Pyruvate carboxylase deficiency involves sequencing the entire PC gene to identify any mutations or variations that may be present. This test can help diagnose individuals with PC deficiency and determine the specific genetic cause of the condition. NGS technology allows for the simultaneous analysis of multiple genes, making it a powerful tool for identifying genetic mutations associated with various disorders.

This test can provide valuable information for individuals and their families, allowing for early diagnosis, appropriate management, and genetic counseling.

Test Name PC Gene Pyruvate carboxylase deficiency 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 PC Gene Pyruvate carboxylase deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with PC Gene Pyruvate carboxylase deficiency
Test Details

PC Gene Pyruvate carboxylase deficiency NGS Genetic Test is a genetic test that uses Next-Generation Sequencing (NGS) technology to analyze the PC gene for mutations associated with Pyruvate Carboxylase (PC) deficiency.

Pyruvate Carboxylase deficiency is a rare genetic disorder that affects the body’s ability to convert pyruvate into energy. This deficiency can lead to a variety of symptoms, including developmental delays, neurological problems, and metabolic disturbances.

The NGS Genetic Test for PC Gene Pyruvate Carboxylase deficiency involves sequencing the entire PC gene to identify any mutations or variations that may be present. This test can help diagnose individuals with PC deficiency and determine the specific genetic cause of the condition.

NGS technology allows for the simultaneous analysis of multiple genes, making it a powerful tool for identifying genetic mutations associated with various disorders. This test can provide valuable information for individuals and their families, allowing for early diagnosis, appropriate management, and genetic counseling.

SKU: TEST-1953 Category:

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