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CHRND Gene Myasthenic Syndrome Congenital Type 3B Fast-Channel Genetic Test Cost

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

-21%

The CHRND Gene Myasthenic Syndrome Congenital Type 3B Fast-Channel Genetic Test is a specialized diagnostic assessment offered by DNA Labs UAE, designed to identify mutations in the CHRND gene. This gene plays a crucial role in the proper functioning of the neuromuscular junction, which is essential for muscle contractions. Mutations in the CHRND gene can lead to Congenital Myasthenic Syndrome Type 3B, a rare disorder characterized by muscle weakness and fatigue, with symptoms often appearing at birth or early childhood.

This specific test targets the fast-channel form of the condition, where the communication between nerves and muscles is impaired due to alterations in the acetylcholine receptor at the neuromuscular junction. By analyzing the genetic makeup of an individual, this test can confirm the presence of CHRND gene mutations, providing essential information for accurate diagnosis, management, and treatment planning.

The cost of the CHRND Gene Myasthenic Syndrome Congenital Type 3B Fast-Channel Genetic Test at DNA Labs UAE is 4400 AED. This investment includes the comprehensive analysis necessary to detect the genetic underpinnings of this condition, offering patients and their families critical insights into their health and guiding healthcare professionals in delivering personalized care strategies.

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CHRND Gene Myasthenic Syndrome Congenital Type 3B Fast-Channel Genetic Test

Welcome to DNA Labs UAE, a leading genetic lab offering advanced genetic testing services. In this blog post, we will discuss the CHRND Gene Myasthenic Syndrome Congenital Type 3B Fast-Channel Genetic Test.

Test Name

CHRND Gene Myasthenic Syndrome Congenital Type 3B Fast-Channel Genetic Test

Components

This test includes the following 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: Neurological Disorders
  • Doctor: Neurologist
  • Test Department: Genetics

Pre Test Information

Before undergoing the CHRND Gene Myasthenic Syndrome Congenital Type 3B Fast-Channel Genetic Test, it is important to provide the following:

  • Clinical History of the Patient who is going for the test
  • A Genetic Counselling session to draw a pedigree chart of family members affected with CHRND Gene Myasthenic Syndrome Congenital Type 3B Fast-Channel

Test Details

The CHRND gene is associated with a specific type of congenital myasthenic syndrome known as congenital myasthenic syndrome type 3B. This syndrome is characterized by a fast-channel defect in the acetylcholine receptor at the neuromuscular junction.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously to identify genetic variations or mutations that may be associated with a particular condition. In the case of CHRND gene myasthenic syndrome, NGS genetic testing can be used to identify any mutations or variations in the CHRND gene that may be causing the condition.

By performing NGS genetic testing, healthcare professionals can obtain detailed genetic information that can aid in the diagnosis, management, and treatment of individuals with congenital myasthenic syndrome type 3B. This information can also be useful for genetic counseling and family planning purposes.

Test Name CHRND Gene Myasthenic syndrome congenital type 3B fast-channel 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 CHRND Gene Myasthenic syndrome, congenital, type 3B, fast-channel NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with CHRND Gene Myasthenic syndrome, congenital, type 3B, fast-channel
Test Details

The CHRND gene is associated with a specific type of congenital myasthenic syndrome, known as congenital myasthenic syndrome type 3B. This type of myasthenic syndrome is characterized by a fast-channel defect in the acetylcholine receptor at the neuromuscular junction.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously to identify genetic variations or mutations that may be associated with a particular condition. In the case of CHRND gene myasthenic syndrome, NGS genetic testing can be used to identify any mutations or variations in the CHRND gene that may be causing the condition.

By performing NGS genetic testing, healthcare professionals can obtain detailed genetic information that can aid in the diagnosis, management, and treatment of individuals with congenital myasthenic syndrome type 3B. This information can also be useful for genetic counseling and family planning purposes.

SKU: TEST-1781 Category:

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