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HSPB8 Gene Neuronopathy Distal Hereditary Motor Type 2A Genetic Test Cost

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

-21%

The HSPB8 gene neuronopathy distal hereditary motor type 2A (dHMN2A) genetic test is a specialized diagnostic tool used to identify mutations in the HSPB8 gene, which are associated with distal hereditary motor neuronopathy type 2A. This condition is a rare genetic disorder characterized by progressive weakness and atrophy of the muscles in the hands and feet, often leading to significant disability. The test is crucial for confirming the diagnosis, understanding the inheritance pattern, and guiding management and treatment options for affected individuals.

Performed at DNA Labs UAE, the test involves analyzing the patient’s DNA to look for specific genetic alterations in the HSPB8 gene that are known to cause dHMN2A. This is achieved through advanced genetic sequencing techniques that ensure accuracy and reliability of the results. The cost of the test is 4400 AED, which reflects the comprehensive nature of the genetic analysis and the expertise required to interpret the results.

By identifying the genetic basis of the condition, the test not only helps in confirming the diagnosis but also assists in family planning and provides insights into the prognosis of the disorder. It is a vital tool for healthcare professionals managing patients with suspected dHMN2A, enabling them to offer personalized care and support to individuals and their families affected by this challenging condition.

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HSPB8 Gene Neuronopathy distal hereditary motor type 2A 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: Neurological Disorders
  • Doctor: Neurologist
  • Test Department: Genetics

Pre Test Information

Clinical History of Patient who is going for HSPB8 Gene Neuronopathy distal hereditary motor type 2A NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with HSPB8 Gene Neuronopathy distal hereditary motor type 2A.

Test Details

HSPB8 Gene Neuronopathy distal hereditary motor type 2A NGS Genetic Test is a genetic test that analyzes the HSPB8 gene for mutations associated with distal hereditary motor neuropathy type 2A (dHMN2A). Distal hereditary motor neuropathy (dHMN) is a group of genetic disorders that primarily affect the motor neurons in the distal parts of the limbs, leading to muscle weakness and wasting. dHMN2A is specifically caused by mutations in the HSPB8 gene, which encodes a protein called heat shock protein beta-8 (HSPB8).

NGS (Next-Generation Sequencing) technology is used in this genetic test to analyze the entire coding region of the HSPB8 gene and identify any mutations or genetic variants that may be present. This comprehensive analysis allows for a more accurate diagnosis of dHMN2A and helps in understanding the underlying genetic cause of the condition.

The HSPB8 Gene Neuronopathy distal hereditary motor type 2A NGS Genetic Test is typically recommended for individuals with symptoms suggestive of dHMN2A, such as progressive muscle weakness and wasting in the distal limbs. It can also be used for carrier testing in individuals with a family history of dHMN2A. The test results can provide valuable information for genetic counseling, family planning, and personalized management of the condition.

It is important to note that this test specifically targets the HSPB8 gene and does not analyze other genes associated with dHMN or other types of motor neuron diseases.

Test Name HSPB8 Gene Neuronopathy distal hereditary motor type 2A 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 HSPB8 Gene Neuronopathy distal hereditary motor type 2A NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with HSPB8 Gene Neuronopathy distal hereditary motor type 2A
Test Details

HSPB8 Gene Neuronopathy distal hereditary motor type 2A NGS Genetic Test is a genetic test that analyzes the HSPB8 gene for mutations associated with distal hereditary motor neuropathy type 2A (dHMN2A).

Distal hereditary motor neuropathy (dHMN) is a group of genetic disorders that primarily affect the motor neurons in the distal parts of the limbs, leading to muscle weakness and wasting. dHMN2A is specifically caused by mutations in the HSPB8 gene, which encodes a protein called heat shock protein beta-8 (HSPB8).

NGS (Next-Generation Sequencing) technology is used in this genetic test to analyze the entire coding region of the HSPB8 gene and identify any mutations or genetic variants that may be present. This comprehensive analysis allows for a more accurate diagnosis of dHMN2A and helps in understanding the underlying genetic cause of the condition.

The HSPB8 Gene Neuronopathy distal hereditary motor type 2A NGS Genetic Test is typically recommended for individuals with symptoms suggestive of dHMN2A, such as progressive muscle weakness and wasting in the distal limbs. It can also be used for carrier testing in individuals with a family history of dHMN2A.

The test results can provide valuable information for genetic counseling, family planning, and personalized management of the condition. It is important to note that this test specifically targets the HSPB8 gene and does not analyze other genes associated with dHMN or other types of motor neuron diseases.

SKU: TEST-1854 Category:

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