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GNPTG Gene Mucolipidosis Type 3 Gamma Genetic Test Cost

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

-21%

The GNPTG gene mucolipidosis type 3 gamma genetic test is a specialized diagnostic procedure aimed at identifying mutations in the GNPTG gene, which are linked to mucolipidosis type III gamma (MLIII gamma), a rare lysosomal storage disorder. This condition affects various bodily systems, leading to symptoms like skeletal abnormalities, joint stiffness, and developmental delays. Early detection through this genetic test can facilitate appropriate management and intervention strategies to improve the quality of life for affected individuals.

Conducted at DNA Labs UAE, a reputable facility known for its advanced genetic testing capabilities, this test offers a reliable means for diagnosing MLIII gamma. The cost of the test is set at 4400 AED, reflecting the comprehensive nature of the analysis and the specialized expertise required to interpret the results. By opting for this test, patients and their families can gain valuable insights into the genetic underpinnings of mucolipidosis type III gamma, paving the way for tailored treatment approaches and genetic counseling.

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GNPTG Gene Mucolipidosis Type 3 Gamma Genetic Test

At DNA Labs UAE, we offer the GNPTG Gene Mucolipidosis Type 3 Gamma Genetic Test at a cost of AED 4400.0.

Test Details

The GNPTG gene is associated with a rare genetic disorder called mucolipidosis type 3 gamma (MLIII gamma). This condition is characterized by progressive skeletal abnormalities, intellectual disability, and delayed development.

Our test utilizes Next-Generation Sequencing (NGS) technology, which allows for the simultaneous analysis of multiple genes. By analyzing the GNPTG gene, we can identify mutations or variations that may be responsible for MLIII gamma. This information is crucial for confirming a diagnosis and providing valuable insights for genetic counseling and management of the condition.

In addition, our test can be used for carrier testing in families with a history of MLIII gamma.

Test Components

  • Price: AED 4400.0
  • Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
  • Report Delivery: 3 to 4 Weeks
  • Method: NGS Technology
  • Test Type: Metabolic Disorders
  • Doctor: General Physician
  • Test Department: Genetics

Pre Test Information

Prior to the test, it is important to provide the clinical history of the patient who will undergo the GNPTG Gene Mucolipidosis Type 3 Gamma NGS Genetic DNA Test. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by Mucolipidosis type 3 gamma.

Please note that NGS testing should be ordered and interpreted by healthcare professionals with expertise in genetics, as it is typically performed by specialized laboratories.

Test Name GNPTG Gene Mucolipidosis type 3 gamma 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 Metabolic Disorders
Doctor General Physician
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for GNPTG Gene Mucolipidosis type 3 gamma NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Mucolipidosis type 3 gamma
Test Details

The GNPTG gene is associated with a condition called mucolipidosis type 3 gamma (MLIII gamma). MLIII gamma is a rare genetic disorder characterized by progressive skeletal abnormalities, intellectual disability, and delayed development.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. In the case of MLIII gamma, NGS testing can be used to identify mutations or variations in the GNPTG gene that may be responsible for the condition.

By identifying specific genetic variants in the GNPTG gene, NGS testing can help confirm a diagnosis of MLIII gamma and provide valuable information for genetic counseling and management of the condition. It can also be used for carrier testing in families with a history of MLIII gamma.

It’s important to note that NGS testing is typically performed by specialized laboratories and should be ordered and interpreted by healthcare professionals with expertise in genetics.