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C19orf12 Gene SPG43 Genetic Test Cost

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

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The C19orf12 gene, associated with the condition known as Spastic Paraplegia 43 (SPG43), is a critical genetic marker for diagnosing this rare hereditary spastic paraplegia. The SPG43 genetic test specifically targets mutations within the C19orf12 gene to confirm the diagnosis, allowing for appropriate management and genetic counseling. DNA Labs UAE offers this specialized genetic test for individuals suspected of having SPG43. The test is priced at 4400 AED, reflecting the advanced molecular techniques employed to accurately identify mutations in the C19orf12 gene. This test is crucial for families seeking answers to genetic conditions, providing them with the necessary information to understand their genetic health better.

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C19orf12 Gene SPG43 Genetic Test Cost

Welcome to the DNA Labs UAE blog! Today, we will be discussing the C19orf12 Gene SPG43 Genetic Test, its cost, symptoms, diagnosis, and more.

Test Details

The C19orf12 gene is associated with a condition called SPG43, which stands for hereditary spastic paraplegia type 43. This rare genetic disorder affects the nervous system, specifically the motor neurons in the spinal cord. It leads to progressive muscle weakness and stiffness in the lower limbs, resulting in difficulty walking.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze a person’s DNA sequence. It allows for the simultaneous analysis of multiple genes, including the C19orf12 gene, to identify any genetic variations or mutations that may be associated with SPG43. This type of testing can help confirm a diagnosis of SPG43 and provide information about the specific genetic changes involved.

Test Components and Price

  • Test Name: C19orf12 Gene SPG43 Genetic Test
  • Components: NGS Technology
  • Price: 4400.0 AED

Sample Condition and Report Delivery

The sample condition required for the C19orf12 Gene SPG43 Genetic Test is blood or extracted DNA. Alternatively, one drop of blood on an FTA Card can also be used. The report delivery time is approximately 3 to 4 weeks.

Test Type and Doctor

The C19orf12 Gene SPG43 Genetic Test falls under the category of Neurological Disorders. It is recommended to consult a Neurologist for this test.

Test Department and Pre Test Information

The C19orf12 Gene SPG43 Genetic Test is conducted in the Genetics department. Before undergoing the test, it is essential to provide the clinical history of the patient who is going for the test. Additionally, a Genetic Counselling session may be conducted to draw a pedigree chart of family members affected with C19orf12 Gene SPG43.

Importance of Genetic Testing for SPG43

Genetic testing for SPG43 can be useful for individuals who have symptoms consistent with the condition and for their family members who may be at risk of inheriting the genetic mutation. The results of the genetic test can help with making an accurate diagnosis, providing genetic counseling, and guiding treatment options and management strategies.

It is important to note that genetic testing should be performed by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate guidance and support.

Thank you for reading our blog on the C19orf12 Gene SPG43 Genetic Test. If you have any further questions or would like to schedule an appointment, please contact DNA Labs UAE.

Test Name C19orf12 Gene SPG43 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 C19orf12 Gene SPG43 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with C19orf12 Gene SPG43
Test Details

The C19orf12 gene is associated with a condition called SPG43, which stands for hereditary spastic paraplegia type 43. This condition is a rare genetic disorder that affects the nervous system, specifically the motor neurons in the spinal cord. It leads to progressive muscle weakness and stiffness in the lower limbs, resulting in difficulty walking.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze a person’s DNA sequence. It allows for the simultaneous analysis of multiple genes, including the C19orf12 gene, to identify any genetic variations or mutations that may be associated with SPG43. This type of testing can help confirm a diagnosis of SPG43 and provide information about the specific genetic changes involved.

Genetic testing for SPG43 can be useful for individuals who have symptoms consistent with the condition and for their family members who may be at risk of inheriting the genetic mutation. The results of the genetic test can help with making an accurate diagnosis, providing genetic counseling, and guiding treatment options and management strategies.

It is important to note that genetic testing should be performed by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate guidance and support.

SKU: TEST-2008 Category:

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