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PRDM12 Gene HSAN8 Genetic Test

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

-21%

The PRDM12 Gene HSAN8 Genetic Test is a specialized diagnostic tool designed to detect mutations in the PRDM12 gene, which are associated with Hereditary Sensory and Autonomic Neuropathy Type VIII (HSAN8). HSAN8 is a rare genetic disorder characterized by severe pain insensitivity, inability to sweat, and other sensory and autonomic nervous system dysfunctions. The test aims to provide crucial information for the accurate diagnosis of HSAN8, enabling appropriate management and counseling for affected individuals and their families.

Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the test involves analyzing the patient’s DNA to identify mutations in the PRDM12 gene. This comprehensive analysis helps in confirming the diagnosis of HSAN8, which is essential for guiding treatment decisions and offering genetic counseling. The cost of the PRDM12 Gene HSAN8 Genetic Test is 4400 AED, reflecting the intricate technology and expertise required to accurately identify the genetic variations associated with this condition.

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  • This test is not intended for medical diagnosis or treatment
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PRDM12 Gene HSAN8 Genetic Test

Components: PRDM12 Gene HSAN8 Genetic Test

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 PRDM12 Gene HSAN8 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PRDM12 Gene HSAN8.

Test Details: The PRDM12 gene is associated with a condition called hereditary sensory and autonomic neuropathy type 8 (HSAN8). HSAN8 is a rare genetic disorder that affects the sensory and autonomic nerves, leading to a loss of sensation, particularly in the hands and feet, as well as problems with the autonomic nervous system. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes, including the PRDM12 gene. NGS technology can analyze the entire coding region of the PRDM12 gene to identify any mutations or variants that may be present. NGS genetic testing for the PRDM12 gene can be useful in diagnosing HSAN8 and determining the specific genetic cause of the condition. It can also be used for carrier testing in individuals with a family history of HSAN8, as well as for prenatal testing in families at risk of having a child with HSAN8. The results of the NGS genetic test for the PRDM12 gene can help guide medical management and treatment decisions for individuals with HSAN8. It can also provide valuable information for genetic counseling and family planning purposes.

Test Name PRDM12 Gene HSAN8 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 PRDM12 Gene HSAN8 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with PRDM12 Gene HSAN8
Test Details

The PRDM12 gene is associated with a condition called hereditary sensory and autonomic neuropathy type 8 (HSAN8). HSAN8 is a rare genetic disorder that affects the sensory and autonomic nerves, leading to a loss of sensation, particularly in the hands and feet, as well as problems with the autonomic nervous system.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes, including the PRDM12 gene. NGS technology can analyze the entire coding region of the PRDM12 gene to identify any mutations or variants that may be present.

NGS genetic testing for the PRDM12 gene can be useful in diagnosing HSAN8 and determining the specific genetic cause of the condition. It can also be used for carrier testing in individuals with a family history of HSAN8, as well as for prenatal testing in families at risk of having a child with HSAN8.

The results of the NGS genetic test for the PRDM12 gene can help guide medical management and treatment decisions for individuals with HSAN8. It can also provide valuable information for genetic counseling and family planning purposes.