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CHKB Gene Muscular Dystrophy Congenital Megaconial Type Genetic Test Cost

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

-21%

The CHKB Gene Muscular Dystrophy Congenital Megaconial Type Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the CHKB gene, which are linked to a rare form of muscular dystrophy known as congenital megaconial type. This condition is characterized by muscle weakness, developmental delays, and distinctive enlarged mitochondria (megaconia) in muscle cells, leading to a range of physical and possibly cognitive impairments.

The test, priced at 4400 AED, involves collecting a DNA sample from the patient, typically through a blood draw or cheek swab, which is then analyzed in the laboratory using advanced genetic sequencing techniques. By examining the specific genetic makeup of the CHKB gene, specialists can confirm a diagnosis of congenital megaconial muscular dystrophy, allowing for early intervention, personalized treatment plans, and genetic counseling for families.

Given the complexity and rarity of this condition, the CHKB gene test is a crucial resource for individuals exhibiting symptoms or with a family history of muscular dystrophy, providing them with essential information for managing the disease. DNA Labs UAE, with its state-of-the-art facilities and expert team, ensures accurate and reliable testing results, contributing significantly to the understanding and treatment of this genetic disorder.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
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CHKB Gene Muscular Dystrophy Congenital Megaconial Type Genetic Test

At DNA Labs UAE, we offer the CHKB Gene Muscular Dystrophy Congenital Megaconial Type Genetic Test at a cost of 4400.0 AED. This test is used to diagnose and identify the specific genetic changes associated with this type of muscular dystrophy.

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: Neurological Disorders
  • Doctor: Neurologist
  • Test Department: Genetics

Pre Test Information

Before undergoing the CHKB Gene Muscular Dystrophy Congenital Megaconial Type Genetic 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 this condition.

Test Details

The CHKB gene is associated with a type of muscular dystrophy known as congenital megaconial muscular dystrophy. This condition is characterized by muscle weakness and wasting, particularly in the limbs and face. It is typically present from birth or early childhood.

NGS genetic testing, or Next-Generation Sequencing, is a high-throughput method used to analyze multiple genes simultaneously. In the context of muscular dystrophy, NGS testing can identify mutations or variations in the CHKB gene that may be causing the condition. By analyzing the individual’s DNA, NGS testing provides information about specific genetic changes that may be responsible for the disease.

Accurate diagnosis, prognosis, and potential treatment options can be determined through NGS testing. It is essential to consult with a healthcare professional or genetic counselor to fully understand the implications and limitations of genetic testing and to interpret the results accurately.

Test Name CHKB Gene Muscular dystrophy congenital megaconial type 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 CHKB Gene Muscular dystrophy, congenital, megaconial type NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with CHKB Gene Muscular dystrophy, congenital, megaconial type
Test Details

The CHKB gene is associated with a type of muscular dystrophy called congenital megaconial muscular dystrophy. This condition is characterized by muscle weakness and wasting, particularly in the limbs and face. It is usually present from birth or early childhood.

NGS genetic testing refers to Next-Generation Sequencing, a high-throughput method used to analyze multiple genes simultaneously. In the context of muscular dystrophy, NGS testing can be used to identify mutations or variations in the CHKB gene that may be causing the condition.

By analyzing the individual’s DNA, NGS testing can provide information about specific genetic changes that may be responsible for the disease. This can help with accurate diagnosis, prognosis, and potential treatment options.

It is important to consult with a healthcare professional or genetic counselor to understand the implications and limitations of genetic testing and to interpret the results accurately.

SKU: TEST-1751 Category:

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