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MOCS1 Gene Molybdenum Cofactor Deficiency Type A Genetic Test Cost

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

-21%

The MOCS1 Gene Molybdenum Cofactor Deficiency Type A Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the MOCS1 gene, which are linked to Molybdenum Cofactor Deficiency (MoCD) Type A. This rare, autosomal recessive metabolic disorder is characterized by the body’s inability to produce molybdenum cofactor, essential for the function of certain enzymes. Symptoms can include severe neurological abnormalities, seizures, and developmental delays, often presenting shortly after birth.

The test involves analyzing the patient’s DNA to detect specific genetic mutations in the MOCS1 gene that cause the deficiency. Early and accurate diagnosis through this genetic test is crucial for managing symptoms and improving the quality of life, although treatment options are limited. The test is priced at 4400 AED and is conducted at DNA Labs UAE, a facility renowned for its state-of-the-art genetic testing services. By identifying carriers of the gene mutation, the test also serves as an important tool for genetic counseling and planning for families with a history of the disorder.

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MOCS1 Gene Molybdenum Cofactor Deficiency Type A Genetic Test

At DNA Labs UAE, we offer the MOCS1 Gene Molybdenum Cofactor Deficiency Type A Genetic Test. This test is designed to diagnose molybdenum cofactor deficiency type A, a rare genetic disorder. The test utilizes NGS (Next-Generation Sequencing) technology to analyze the MOCS1 gene and identify any genetic variations or mutations that may be causing the condition.

Test Components and Price

  • Components: MOCS1 Gene Molybdenum Cofactor Deficiency Type A Genetic Test
  • Price: 4400.0 AED

Sample Condition

The test requires a blood sample, extracted DNA, or one drop of blood on an FTA card.

Report Delivery

After the sample is received, the report will be delivered within 3 to 4 weeks.

Method

The test utilizes NGS technology to analyze the MOCS1 gene.

Test Type

The MOCS1 Gene Molybdenum Cofactor Deficiency Type A Genetic Test falls under the category of metabolic disorders.

Doctor

This test can be ordered by a general physician.

Test Department

The MOCS1 Gene Molybdenum Cofactor Deficiency Type A Genetic Test is performed by our Genetics department.

Pre Test Information

Prior to the test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by molybdenum cofactor deficiency type A.

Test Details

Molybdenum cofactor deficiency type A is a rare genetic disorder characterized by the inability to produce a functional molybdenum cofactor. This cofactor is essential for the proper functioning of several enzymes in the body. The MOCS1 Gene Molybdenum Cofactor Deficiency Type A Genetic Test utilizes NGS technology to identify any genetic variations or mutations in the MOCS1 gene that may be causing the condition.

The test not only aids in diagnosing the condition and determining the specific genetic cause but also provides valuable information for genetic counseling and family planning. It can also identify carriers of the MOCS1 gene mutation who may be at risk of passing the condition to their children.

It is important to note that NGS genetic testing requires a DNA sample, typically obtained through a blood or saliva sample. It is recommended to have the test performed by a qualified healthcare professional or genetic testing laboratory. The interpretation of the test results should be done by a healthcare professional specializing in genetics.

Test Name MOCS1 Gene Molybdenum cofactor deficiency type A 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 MOCS1 Gene Molybdenum cofactor deficiency type A NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Molybdenum cofactor deficiency type A
Test Details

The MOCS1 gene is associated with molybdenum cofactor deficiency type A, which is a rare genetic disorder. Molybdenum cofactor deficiency type A is characterized by the inability to produce a functional molybdenum cofactor, which is necessary for the proper functioning of several enzymes in the body.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of MOCS1 gene testing, NGS can be used to identify any genetic variations or mutations in the MOCS1 gene that may be causing molybdenum cofactor deficiency type A.

This type of genetic testing can help in diagnosing the condition, determining the specific genetic cause, and providing information for genetic counseling and family planning. It can also be used to identify carriers of the MOCS1 gene mutation who may be at risk of passing the condition to their children.

It’s important to note that NGS genetic testing requires a DNA sample, typically obtained through a blood or saliva sample, and should be performed by a qualified healthcare professional or genetic testing laboratory. The results of the test should be interpreted by a healthcare professional who specializes in genetics.

SKU: TEST-2553 Category:

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