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MPZ Gene Dejerine-Sottas Disease Genetic Test

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

-21%

The MPZ Gene Dejerine-Sottas Disease Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the MPZ gene associated with Dejerine-Sottas Disease (DSD), also known as hereditary motor and sensory neuropathy type III. DSD is a rare genetic disorder characterized by progressive nerve damage leading to muscle weakness, sensory loss, and in severe cases, disability. The MPZ gene plays a crucial role in the development and function of myelin, the protective sheath surrounding nerve fibers, and mutations in this gene can disrupt nerve signal transmission.

This genetic test involves analyzing the patient’s DNA to detect specific mutations in the MPZ gene that are linked to the development of Dejerine-Sottas Disease. Early diagnosis through this test can be crucial for managing symptoms, implementing appropriate therapies, and providing genetic counseling for affected families.

The test is priced at 4400 AED and is conducted at DNA Labs UAE, which is equipped with state-of-the-art technology and staffed by experienced professionals to ensure accurate and reliable results. Individuals undergoing this test can expect a comprehensive analysis, with results that can guide treatment decisions and offer insights into the hereditary nature of the condition.

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  • This test is not intended for medical diagnosis or treatment
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MPZ Gene Dejerine-Sottas disease Genetic Test

Test Name: MPZ Gene Dejerine-Sottas disease Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

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: Neurological Disorders

Doctor: Neurologist

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for MPZ Gene Dejerine-Sottas disease NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MPZ Gene Dejerine-Sottas disease.

Test Details: Dejerine-Sottas disease is a rare genetic disorder that affects the peripheral nerves. It is caused by mutations in the MPZ gene, which provides instructions for making a protein called myelin protein zero. Myelin protein zero is a critical component of myelin, the fatty substance that surrounds and insulates nerve fibers, allowing them to transmit electrical signals quickly and efficiently. NGS (next-generation sequencing) genetic testing can be used to identify mutations in the MPZ gene that cause Dejerine-Sottas disease. This type of testing involves analyzing the DNA sequence of the gene to look for changes or variations that may disrupt the function of the protein it encodes. NGS is a highly sensitive and accurate method of genetic testing that can detect even very rare mutations. Genetic testing for Dejerine-Sottas disease can be useful for individuals who have symptoms of the condition, as well as for family members of affected individuals who may be at risk of inheriting the disease. Early diagnosis can help to guide treatment and management strategies, as well as provide information about the likelihood of passing the condition on to future generations.

Test Name MPZ Gene Dejerine-Sottas disease Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card o
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Neurological Disorders
Doctor Neurologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for MPZ Gene Dejerine-Sottas disease NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with MPZ Gene Dejerine-Sottas disease
Test Details

Dejerine-Sottas disease is a rare genetic disorder that affects the peripheral nerves. It is caused by mutations in the MPZ gene, which provides instructions for making a protein called myelin protein zero. Myelin protein zero is a critical component of myelin, the fatty substance that surrounds and insulates nerve fibers, allowing them to transmit electrical signals quickly and efficiently.

NGS (next-generation sequencing) genetic testing can be used to identify mutations in the MPZ gene that cause Dejerine-Sottas disease. This type of testing involves analyzing the DNA sequence of the gene to look for changes or variations that may disrupt the function of the protein it encodes. NGS is a highly sensitive and accurate method of genetic testing that can detect even very rare mutations.

Genetic testing for Dejerine-Sottas disease can be useful for individuals who have symptoms of the condition, as well as for family members of affected individuals who may be at risk of inheriting the disease. Early diagnosis can help to guide treatment and management strategies, as well as provide information about the likelihood of passing the condition on to future generations.