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TECPR2 Gene SPG49 Genetic Test Cost

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

-21%

The TECPR2 gene SPG49 genetic test is a specialized diagnostic procedure aimed at detecting mutations in the TECPR2 gene, which are associated with a rare neurodegenerative disorder known as spastic paraplegia 49 (SPG49). This condition is part of a group of genetic disorders known as hereditary spastic paraplegias (HSP), characterized by progressive stiffness and contraction (spasticity) in the lower limbs. SPG49, in particular, is distinguished by additional features that may include intellectual disability, developmental delays, and problems with the autonomic nervous system.

DNA Labs UAE offers this genetic test, providing a critical tool for the accurate diagnosis of SPG49. The test involves analyzing the patient’s DNA to look for specific mutations in the TECPR2 gene that are indicative of the disorder. Early and precise diagnosis through this test can facilitate appropriate clinical management, counseling, and support for affected individuals and their families.

The cost of the TECPR2 gene SPG49 genetic test at DNA Labs UAE is 4400 AED. This price reflects the specialized nature of the test and the comprehensive analysis required to identify the genetic mutations associated with SPG49. Patients interested in undergoing this test are advised to consult with their healthcare provider to understand the implications of the results and to discuss the best course of action based on the outcome.

Description

TECPR2 Gene SPG49 Genetic Test

Cost: AED 4400.0

Symptoms, Diagnosis, and Test Details

The TECPR2 gene is associated with a rare genetic disorder called hereditary spastic paraplegia type 49 (SPG49). This disorder is characterized by progressive stiffness and weakness of the legs, leading to difficulty walking. It is caused by mutations in the TECPR2 gene, which is involved in the transport of proteins within cells.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. In the case of SPG49, NGS genetic testing can be used to identify mutations in the TECPR2 gene.

The purpose of the SPG49 NGS genetic test is to confirm a diagnosis of hereditary spastic paraplegia type 49 by identifying mutations in the TECPR2 gene. This test can help to determine the underlying cause of the symptoms and guide treatment decisions.

It is important to note that genetic testing for SPG49 is typically only ordered for individuals who have symptoms consistent with hereditary spastic paraplegia and a suspected genetic cause. The test may not be necessary or appropriate for individuals without symptoms or a family history of the condition.

Test Components and Price

Test Name: TECPR2 Gene SPG49 Genetic Test
Components: Blood or Extracted DNA or One drop Blood on FTA Card
Price: AED 4400.0

Sample Condition and Report Delivery

Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery: 3 to 4 Weeks

Method and Test Type

Method: NGS Technology
Test Type: Neurological Disorders

Referring Doctor and Test Department

Doctor: Neurologist
Test Department: Genetics

Pre Test Information

Clinical History of Patient who is going for TECPR2 Gene SPG49 NGS Genetic DNA Test

A Genetic Counselling session to draw a pedigree chart of family members affected with TECPR2 Gene SPG49

Consult a Healthcare Professional or Genetic Counselor

If you have concerns about hereditary spastic paraplegia type 49 or believe you may be at risk, it is recommended to consult with a healthcare professional or a genetic counselor who can provide more information and guidance regarding genetic testing options.

Test Name	TECPR2 Gene SPG49 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 TECPR2 Gene SPG49 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with TECPR2 Gene SPG49
Test Details	The TECPR2 gene is associated with a rare genetic disorder called hereditary spastic paraplegia type 49 (SPG49). This disorder is characterized by progressive stiffness and weakness of the legs, leading to difficulty walking. It is caused by mutations in the TECPR2 gene, which is involved in the transport of proteins within cells. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. In the case of SPG49, NGS genetic testing can be used to identify mutations in the TECPR2 gene. The purpose of the SPG49 NGS genetic test is to confirm a diagnosis of hereditary spastic paraplegia type 49 by identifying mutations in the TECPR2 gene. This test can help to determine the underlying cause of the symptoms and guide treatment decisions. It is important to note that genetic testing for SPG49 is typically only ordered for individuals who have symptoms consistent with hereditary spastic paraplegia and a suspected genetic cause. The test may not be necessary or appropriate for individuals without symptoms or a family history of the condition. If you have concerns about hereditary spastic paraplegia type 49 or believe you may be at risk, it is recommended to consult with a healthcare professional or a genetic counselor who can provide more information and guidance regarding genetic testing options.

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