GM2 Gangliosidosis Quantitative Blood Tay Sachs and Sandhoff Disease Test sale cost 560 AED
Galactosemia Epimerase Quantitative Blood Test sale cost 570 AED Galactosemia Epimerase Quantitative Blood Test Cost 640 د.إ Original price was: 640 د.إ.570 د.إCurrent price is: 570 د.إ.
Niemann Pick Disease Quantitative Blood Test sale cost 510 AED Niemann Pick Disease Quantitative Blood Test Cost 570 د.إ Original price was: 570 د.إ.510 د.إCurrent price is: 510 د.إ.
Sale!

GM2 Gangliosidosis Quantitative Blood Tay Sachs and Sandhoff Disease Test Cost

Original price was: 620 د.إ.Current price is: 560 د.إ.

-10%

GM2 Gangliosidosis is a group of genetic disorders that include Tay-Sachs Disease and Sandhoff Disease. These conditions are characterized by the accumulation of certain lipids in the brain, leading to progressive neurodegeneration. The cause of these diseases is a deficiency in the enzymes required to break down these lipids. Tay-Sachs Disease is primarily caused by a deficiency in the Hexosaminidase A enzyme, while Sandhoff Disease results from a deficiency in both the Hexosaminidase A and B enzymes.

The GM2 Gangliosidosis Quantitative Blood Test is a specialized diagnostic test designed to measure the activity levels of these crucial enzymes in the blood. By assessing the activity of Hexosaminidase A and B, this test can help in the diagnosis of Tay-Sachs Disease, Sandhoff Disease, and related genetic conditions. It is an essential tool for early detection, allowing for timely intervention and management of these disorders.

DNA Labs UAE offers the GM2 Gangliosidosis Quantitative Blood Test for individuals who may be at risk of these conditions or exhibit symptoms suggestive of these diseases. The cost of the test is 560 AED. Conducting the test in a reputable laboratory like DNA Labs UAE ensures accuracy and reliability of results, providing crucial information for affected individuals and their families. This test is an important step in the management and understanding of Tay-Sachs and Sandhoff Disease, offering hope for better outcomes through early diagnosis and intervention.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
Guaranteed Safe Checkout

GM2 Gangliosidosis Quantitative Blood Test

Welcome to DNA Labs UAE, a leading genetic lab specializing in diagnostic testing. Today, we will be discussing the GM2 Gangliosidosis Quantitative Blood Test, specifically focusing on Tay-Sachs disease and Sandhoff disease. These genetic disorders result in the accumulation of GM2 gangliosides in the body, leading to neurological symptoms and developmental regression.

Test Details

The GM2 Gangliosidosis Quantitative Blood Test is a diagnostic test used to measure the levels of GM2 gangliosides in the blood. This test involves drawing a blood sample from the patient and analyzing it in our state-of-the-art laboratory. The test specifically measures the levels of GM2 ganglioside A and GM2 ganglioside B.

Test Components

  • Test Name: GM2 Gangliosidosis Quantitative Blood Tay-Sachs and Sandhoff Disease Test
  • Price: 560.0 AED
  • Sample Condition: 10 ml (7.5 mL min.) whole blood from 3 Lavender Top (EDTA) / Green Top (Sodium heparin) tubes. Ship refrigerated. DO NOT FREEZE. Clinical details must accompany sample.
  • Report Delivery: Sample daily by 4 pm; Report 4 days
  • Method: Enzyme Assay
  • Test Type: Inborn Errors of Metabolism
  • Doctor: Pediatrician
  • Test Department: Genetic
  • Pre Test Information: Clinical details must accompany sample.

Symptoms and Diagnosis

Tay-Sachs disease and Sandhoff disease are characterized by the progressive destruction of nerve cells in the brain and spinal cord. This leads to neurological symptoms and developmental regression. Symptoms may include muscle weakness, loss of motor skills, seizures, and cognitive decline. Diagnosis of these diseases is crucial for early intervention and management.

Confirmatory Testing

It is important to note that the GM2 Gangliosidosis Quantitative Blood Test is not a definitive diagnostic tool for GM2 gangliosidosis. Further confirmatory testing, such as genetic testing or enzyme activity assays, may be required to confirm the diagnosis.

Monitoring and Treatment

In addition to diagnosis, this blood test can also be used to monitor the progression of the disease and the effectiveness of treatment in individuals already diagnosed with GM2 gangliosidosis. Regular testing and close monitoring are essential for managing these conditions.

At DNA Labs UAE, we are committed to providing accurate and timely genetic testing services. Our team of experts is dedicated to helping healthcare professionals and patients in the diagnosis and management of genetic disorders. Contact us today to learn more about our services and to schedule an appointment for the GM2 Gangliosidosis Quantitative Blood Test.

Test Name GM2 GANGLIOSIDOSIS QUANTITATIVE BLOOD TAY SACHS and SANDHOFF DISEASE Test
Components
Price 560.0 AED
Sample Condition 10 ml (7.5 mL min.) whole blood from 3 Lavender Top (EDTA) \/ Green Top (Sodium heparin) tubes. Ship refrigerated. DO NOT FREEZE. Clinical details must accompany sample.
Report Delivery Sample Daily by 4 pm; Report 4 days
Method Enzyme Assay
Test type Inborn Errors of Metabolism
Doctor Pediatrician
Test Department: GENETIC
Pre Test Information Clinical details must accompany sample.
Test Details

The GM2 gangliosidosis quantitative blood test is a diagnostic test used to measure the levels of GM2 gangliosides in the blood. GM2 gangliosidosis refers to a group of genetic disorders that result in the accumulation of GM2 gangliosides in the cells of the body, particularly in the brain and nervous system.

The test is primarily used to diagnose Tay-Sachs disease and Sandhoff disease, which are two types of GM2 gangliosidosis. These diseases are characterized by the progressive destruction of nerve cells in the brain and spinal cord, leading to neurological symptoms and developmental regression.

The quantitative blood test involves drawing a blood sample from the patient and analyzing it in a laboratory. The test measures the levels of GM2 gangliosides, specifically GM2 ganglioside A and GM2 ganglioside B, in the blood. Elevated levels of these gangliosides indicate a possible diagnosis of Tay-Sachs disease or Sandhoff disease.

It is important to note that this blood test is not a definitive diagnostic tool for GM2 gangliosidosis. Further confirmatory testing, such as genetic testing or enzyme activity assays, may be required to confirm the diagnosis. Additionally, this test may also be used to monitor the progression of the disease and the effectiveness of treatment in individuals already diagnosed with GM2 gangliosidosis.

SKU: TEST-6210 Category:

Related products