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Mucopolysaccharidosis MPS Type VI Maroteaux Lamy Quantitative Blood Test Cost

Original price was: 430 د.إ.Current price is: 380 د.إ.

-12%

The Mucopolysaccharidosis (MPS) Type VI, also known as Maroteaux-Lamy syndrome, is a rare lysosomal storage disorder characterized by the body’s inability to break down certain large molecules known as glycosaminoglycans (GAGs). This inability leads to the accumulation of GAGs within cells, causing various systemic symptoms including skeletal abnormalities, vision and hearing impairment, and cardiovascular issues. The condition is caused by mutations in the ARSB gene, leading to deficient activity of the enzyme arylsulfatase B.

To diagnose MPS Type VI and to help manage its treatment, a quantitative blood test can be utilized. This test measures the activity of the enzyme arylsulfatase B in the blood, providing crucial information for the diagnosis of Maroteaux-Lamy syndrome. Early diagnosis through such testing is essential for the effective management and treatment of the disorder, which may include enzyme replacement therapy and other supportive measures to improve quality of life and reduce the severity of symptoms.

In the United Arab Emirates, DNA Labs UAE offers this vital diagnostic service. The cost for the MPS Type VI Maroteaux-Lamy Quantitative Blood Test at DNA Labs UAE is 380 AED. This facility provides state-of-the-art diagnostic services, ensuring accurate and timely results for patients and healthcare providers, aiding in the early detection and management of this rare condition.

Description

MUCOPOLYSACCHARIDOSIS MPS TYPE VI MAROTEAUX LAMY QUANTITATIVE BLOOD Test

Test Name: MUCOPOLYSACCHARIDOSIS MPS TYPE VI MAROTEAUX LAMY QUANTITATIVE BLOOD Test

Components: Price 380.0 AED

Sample Condition: 10 mL (7.5 mL min.) whole blood from 3 Lavender Top (EDTA) OR Green Top (Sodium Heparin) tubes. Ship refrigerated. DO NOT FREEZE. Provide brief clinical history.

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: Provide brief clinical history.

Test Details:

A quantitative blood test for Mucopolysaccharidosis (MPS) Type VI, also known as Maroteaux-Lamy syndrome, measures the levels of the enzyme arylsulfatase B (ASB) in the blood. MPS Type VI is a rare genetic disorder characterized by the deficiency or malfunctioning of this enzyme, leading to the accumulation of certain complex carbohydrates called glycosaminoglycans (GAGs) in various tissues and organs.

To perform the quantitative blood test, a blood sample is taken from the individual and sent to a laboratory for analysis. The laboratory measures the activity or levels of ASB in the blood using specialized techniques. If the levels of ASB are significantly reduced or absent, it indicates a possible diagnosis of MPS Type VI.

This quantitative blood test helps in the diagnosis and monitoring of MPS Type VI. It can be used to confirm a suspected diagnosis based on clinical symptoms and other diagnostic tests. Additionally, it can be used to assess the effectiveness of enzyme replacement therapy (ERT) in individuals receiving treatment for MPS Type VI.

It is important to note that a quantitative blood test for MPS Type VI is just one component of the diagnostic process. Other diagnostic tests, such as urine analysis, genetic testing, and imaging studies, may also be necessary to confirm the diagnosis and evaluate the extent of organ involvement. A consultation with a medical geneticist or a specialist in metabolic disorders is recommended for accurate diagnosis and management of MPS Type VI.

Test Name	MUCOPOLYSACCHARIDOSIS MPS TYPE VI MAROTEAUX LAMY QUANTITATIVE BLOOD Test
Components
Price	380.0 AED
Sample Condition	10 mL (7.5 mL min.) whole blood from 3 Lavender Top (EDTA)OR Green Top (Sodium Heparin) tubes. Ship refrigerated. DO NOT FREEZE. Provide brief clinical history.
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	Provide brief clinical history.
Test Details	A quantitative blood test for Mucopolysaccharidosis (MPS) Type VI, also known as Maroteaux-Lamy syndrome, measures the levels of the enzyme arylsulfatase B (ASB) in the blood. MPS Type VI is a rare genetic disorder characterized by the deficiency or malfunctioning of this enzyme, leading to the accumulation of certain complex carbohydrates called glycosaminoglycans (GAGs) in various tissues and organs. To perform the quantitative blood test, a blood sample is taken from the individual and sent to a laboratory for analysis. The laboratory measures the activity or levels of ASB in the blood using specialized techniques. If the levels of ASB are significantly reduced or absent, it indicates a possible diagnosis of MPS Type VI. This quantitative blood test helps in the diagnosis and monitoring of MPS Type VI. It can be used to confirm a suspected diagnosis based on clinical symptoms and other diagnostic tests. Additionally, it can be used to assess the effectiveness of enzyme replacement therapy (ERT) in individuals receiving treatment for MPS Type VI. It is important to note that a quantitative blood test for MPS Type VI is just one component of the diagnostic process. Other diagnostic tests, such as urine analysis, genetic testing, and imaging studies, may also be necessary to confirm the diagnosis and evaluate the extent of organ involvement. A consultation with a medical geneticist or a specialist in metabolic disorders is recommended for accurate diagnosis and management of MPS Type VI.