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MCOLN1 Gene Mucolipidosis Type 4 Genetic Test Cost

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

-21%

The MCOLN1 Gene Mucolipidosis Type 4 Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to identify mutations in the MCOLN1 gene, which are associated with Mucolipidosis Type IV. This rare genetic disorder affects the body’s ability to break down and recycle certain materials, leading to severe developmental delays, vision problems, and motor skill impairments. The test, which costs 4400 AED, involves analyzing the patient’s DNA to detect specific genetic alterations in the MCOLN1 gene, providing crucial information for accurate diagnosis and management of the condition. By pinpointing the exact nature of the genetic mutation, healthcare providers can offer targeted treatment plans and support to patients and their families, enhancing the quality of life for those affected by Mucolipidosis Type IV.

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MCOLN1 Gene Mucolipidosis type 4 Genetic Test

Test Name: MCOLN1 Gene Mucolipidosis type 4 Genetic Test

Components: NGS Technology

Price: 4400.0 AED

Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card

Report Delivery: 3 to 4 Weeks

Test Type: Metabolic Disorders

Doctor: General Physician

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for MCOLN1 Gene Mucolipidosis type 4 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Mucolipidosis type 4.

Overview

The MCOLN1 gene is associated with a genetic disorder called Mucolipidosis type 4 (ML4). ML4 is a rare autosomal recessive disorder that affects the lysosomal system, leading to the accumulation of various substances within cells.

NGS Technology

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously to identify genetic variations or mutations. In the context of ML4, NGS genetic testing can be used to identify mutations in the MCOLN1 gene.

By analyzing the MCOLN1 gene, NGS testing can determine if there are any variations or mutations that are associated with ML4. This can help in confirming a diagnosis of ML4 and providing information about the specific mutation(s) present.

NGS genetic testing is a powerful tool in diagnosing genetic disorders like ML4 as it allows for the analysis of multiple genes simultaneously, providing a comprehensive genetic profile. This can help in understanding the underlying cause of the disorder and may also have implications for treatment options and genetic counseling.

Test Name MCOLN1 Gene Mucolipidosis type 4 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 MCOLN1 Gene Mucolipidosis type 4 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Mucolipidosis type 4
Test Details

The MCOLN1 gene is associated with a genetic disorder called Mucolipidosis type 4 (ML4). ML4 is a rare autosomal recessive disorder that affects the lysosomal system, leading to the accumulation of various substances within cells.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously to identify genetic variations or mutations. In the context of ML4, NGS genetic testing can be used to identify mutations in the MCOLN1 gene.

By analyzing the MCOLN1 gene, NGS testing can determine if there are any variations or mutations that are associated with ML4. This can help in confirming a diagnosis of ML4 and providing information about the specific mutation(s) present.

NGS genetic testing is a powerful tool in diagnosing genetic disorders like ML4 as it allows for the analysis of multiple genes simultaneously, providing a comprehensive genetic profile. This can help in understanding the underlying cause of the disorder and may also have implications for treatment options and genetic counseling.