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SPTLC2 Gene Neuropathy Hereditary Sensory and Autonomic Type 1C Genetic Test Cost

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

-21%

The SPTLC2 Gene Neuropathy Hereditary Sensory and Autonomic Type 1C Genetic Test is a specialized diagnostic examination designed to identify mutations in the SPTLC2 gene, which are linked to the development of Hereditary Sensory and Autonomic Neuropathy Type 1C (HSAN1C). This condition is a rare genetic disorder characterized by a loss of sensory and autonomic functions, leading to symptoms such as insensitivity to pain, temperature, and touch, as well as autonomic dysfunctions.

Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, this test involves analyzing the patient’s DNA to detect abnormalities in the SPTLC2 gene that can confirm the diagnosis of HSAN1C. The process is critical for patients exhibiting symptoms of sensory and autonomic neuropathy, as it allows for accurate diagnosis, which is essential for the management and treatment of the condition.

The cost of the SPTLC2 Gene Neuropathy Hereditary Sensory and Autonomic Type 1C Genetic Test at DNA Labs UAE is 4400 AED. This investment in health enables individuals and families affected by this condition to take informed steps towards managing the disorder, potentially improving the quality of life for those diagnosed. Given the complexity and rarity of HSAN1C, accessing precise genetic testing such as this offers a crucial pathway to understanding and addressing this challenging condition.

Description

SPTLC2 Gene Neuropathy hereditary sensory and autonomic type 1C Genetic Test

Test Name: SPTLC2 Gene Neuropathy hereditary sensory and autonomic type 1C Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

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 SPTLC2 Gene Neuropathy, hereditary sensory and autonomic type 1C NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SPTLC2 Gene Neuropathy, hereditary sensory and autonomic type 1C.

Test Details: SPTLC2 gene neuropathy, also known as hereditary sensory and autonomic neuropathy type 1C (HSAN1C), is a rare genetic disorder that affects the peripheral nerves. It is caused by mutations in the SPTLC2 gene, which provides instructions for making an enzyme called serine palmitoyltransferase long chain base subunit 2. This condition is characterized by progressive damage to the sensory and autonomic nerves, leading to various symptoms such as loss of sensation in the hands and feet, muscle weakness, muscle wasting, impaired sweating, and difficulty controlling blood pressure and heart rate. The severity and progression of symptoms can vary among affected individuals.

NGS (Next-Generation Sequencing) genetic testing is a diagnostic method that can identify mutations in the SPTLC2 gene associated with HSAN1C. It involves sequencing the DNA of the individual to detect any changes or variations in the gene sequence. This test can help confirm a diagnosis of HSAN1C and provide valuable information for genetic counseling and management of the condition.

It is important to note that HSAN1C is a rare genetic disorder, and genetic testing may not be readily available in all healthcare settings. A geneticist or genetic counselor can provide more information and guidance on the availability and appropriateness of genetic testing for this condition.

Test Name	SPTLC2 Gene Neuropathy hereditary sensory and autonomic type 1C 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 SPTLC2 Gene Neuropathy, hereditary sensory and autonomic type 1C NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with SPTLC2 Gene Neuropathy, hereditary sensory and autonomic type 1C
Test Details	SPTLC2 gene neuropathy, also known as hereditary sensory and autonomic neuropathy type 1C (HSAN1C), is a rare genetic disorder that affects the peripheral nerves. It is caused by mutations in the SPTLC2 gene, which provides instructions for making an enzyme called serine palmitoyltransferase long chain base subunit 2. This condition is characterized by progressive damage to the sensory and autonomic nerves, leading to various symptoms such as loss of sensation in the hands and feet, muscle weakness, muscle wasting, impaired sweating, and difficulty controlling blood pressure and heart rate. The severity and progression of symptoms can vary among affected individuals. NGS (Next-Generation Sequencing) genetic testing is a diagnostic method that can identify mutations in the SPTLC2 gene associated with HSAN1C. It involves sequencing the DNA of the individual to detect any changes or variations in the gene sequence. This test can help confirm a diagnosis of HSAN1C and provide valuable information for genetic counseling and management of the condition. It is important to note that HSAN1C is a rare genetic disorder, and genetic testing may not be readily available in all healthcare settings. A geneticist or genetic counselor can provide more information and guidance on the availability and appropriateness of genetic testing for this condition.