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IDUA Gene Mucopolysaccharidosis Type 1H Genetic Test Cost

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

-21%

The IDUA Gene Mucopolysaccharidosis Type 1H Genetic Test is a specialized diagnostic procedure designed to detect mutations in the IDUA gene, which are responsible for causing Mucopolysaccharidosis Type 1H (MPS 1H), also known as Hurler syndrome. This condition is a rare, inherited lysosomal storage disorder characterized by the body’s inability to break down certain long chains of sugar molecules called glycosaminoglycans. The accumulation of these molecules in various body tissues leads to a range of symptoms including developmental delay, skeletal and joint abnormalities, and organ dysfunction.

The test involves analyzing the patient’s DNA, extracted from a blood sample, to identify any mutations in the IDUA gene that are indicative of MPS 1H. It is a crucial tool for early diagnosis, which can significantly impact the management and treatment of the disease, potentially improving the quality of life and lifespan of affected individuals.

The IDUA Gene Mucopolysaccharidosis Type 1H Genetic Test is available at DNA Labs UAE, a leading facility in genetic testing and personalized medicine. The cost of the test is 4400 AED, reflecting the specialized nature of the analysis and the sophisticated technology employed. Early diagnosis through this test can facilitate timely intervention and access to supportive therapies, making it a valuable resource for families with a history of MPS 1H.

Description

IDUA Gene Mucopolysaccharidosis type 1H Genetic Test

Components: IDUA Gene Mucopolysaccharidosis type 1H 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: Metabolic Disorders

Doctor: General Physician

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for IDUA Gene Mucopolysaccharidosis type 1H NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Mucopolysaccharidosis type 1H.

Test Details: The IDUA gene is associated with Mucopolysaccharidosis type 1H (MPS 1H), also known as Hurler syndrome. MPS 1H is a rare genetic disorder characterized by the deficiency of the enzyme alpha-L-iduronidase, which leads to the buildup of certain substances called glycosaminoglycans in the body’s cells and tissues. NGS (Next-Generation Sequencing) Genetic Test refers to a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the context of MPS 1H, an NGS genetic test would involve sequencing the IDUA gene to identify any disease-causing mutations or variants. This type of genetic testing can help diagnose MPS 1H, confirm a suspected diagnosis, or identify carriers of the condition. It may also be used for prenatal testing or for screening family members of an affected individual. It is important to note that genetic testing for MPS 1H should be performed and interpreted by a qualified healthcare professional or genetic counselor, as the results can have significant implications for the individual and their family.

Test Name	IDUA Gene Mucopolysaccharidosis type 1H 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 IDUA Gene Mucopolysaccharidosis type 1H NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Mucopolysaccharidosis type 1H
Test Details	The IDUA gene is associated with Mucopolysaccharidosis type 1H (MPS 1H), also known as Hurler syndrome. MPS 1H is a rare genetic disorder characterized by the deficiency of the enzyme alpha-L-iduronidase, which leads to the buildup of certain substances called glycosaminoglycans in the body’s cells and tissues. NGS (Next-Generation Sequencing) Genetic Test refers to a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the context of MPS 1H, an NGS genetic test would involve sequencing the IDUA gene to identify any disease-causing mutations or variants. This type of genetic testing can help diagnose MPS 1H, confirm a suspected diagnosis, or identify carriers of the condition. It may also be used for prenatal testing or for screening family members of an affected individual. It is important to note that genetic testing for MPS 1H should be performed and interpreted by a qualified healthcare professional or genetic counselor, as the results can have significant implications for the individual and their family.