Sale!

PEX11B Gene Peroxisome Biogenesis Disorder 14B Genetic Test Cost

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

-21%

The PEX11B Gene Peroxisome Biogenesis Disorder 14B Genetic Test is a specialized diagnostic examination offered by DNA Labs UAE, designed to identify mutations in the PEX11B gene, which are linked to Peroxisome Biogenesis Disorder 14B (PBD14B). This rare genetic condition affects the body’s ability to properly form and function peroxisomes, essential cellular components involved in various critical biochemical pathways, including lipid metabolism and the detoxification of harmful substances.

PBD14B manifests with a spectrum of clinical features, ranging from severe neurological impairments to more subtle physiological anomalies, depending on the nature and extent of the genetic mutation. Early and accurate diagnosis through the PEX11B gene test can facilitate timely intervention and management strategies, potentially improving the quality of life for affected individuals.

The test is conducted with a sample of the patient’s DNA, extracted from a blood sample or cheek swab, and analyzed using advanced genetic sequencing techniques to detect mutations in the PEX11B gene. The cost of the test is 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify the genetic alterations associated with this disorder.

DNA Labs UAE is at the forefront of genetic testing, offering this critical diagnostic tool as part of its comprehensive suite of genetic services. By providing this test, DNA Labs UAE supports the early detection and management of Peroxisome Biogenesis Disorder 14B, contributing to the broader effort to combat rare genetic diseases.

Description

PEX11B Gene Peroxisome Biogenesis Disorder 14B Genetic Test

Components: PEX11B Gene Peroxisome biogenesis disorder 14B 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 PEX11B Gene Peroxisome biogenesis disorder 14B NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PEX11B Gene Peroxisome biogenesis disorder 14B

Test Details:

The PEX11B gene is associated with peroxisome biogenesis disorder 14B (PBD14B), which is a rare genetic disorder characterized by the impaired development and function of peroxisomes. Peroxisomes are cellular structures involved in various metabolic processes, including the breakdown of fatty acids and the detoxification of harmful substances.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of PBD14B, NGS genetic testing can be used to identify mutations or variants in the PEX11B gene that may be causing the disorder.

By analyzing the genetic information obtained through NGS, healthcare professionals can diagnose PBD14B, provide genetic counseling, and potentially offer personalized treatment options. It can also help in understanding the inheritance pattern of the disorder and assessing the risk of passing it on to future generations.

It is important to note that NGS genetic testing should be performed and interpreted by qualified healthcare professionals who specialize in genetics or genetic counseling. They can provide appropriate guidance and support to individuals and families undergoing genetic testing for PBD14B or any other genetic disorder.

Test Name	PEX11B Gene Peroxisome biogenesis disorder 14B 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 PEX11B Gene Peroxisome biogenesis disorder 14B NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with PEX11B Gene Peroxisome biogenesis disorder 14B
Test Details	The PEX11B gene is associated with peroxisome biogenesis disorder 14B (PBD14B), which is a rare genetic disorder characterized by the impaired development and function of peroxisomes. Peroxisomes are cellular structures involved in various metabolic processes, including the breakdown of fatty acids and the detoxification of harmful substances. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of PBD14B, NGS genetic testing can be used to identify mutations or variants in the PEX11B gene that may be causing the disorder. By analyzing the genetic information obtained through NGS, healthcare professionals can diagnose PBD14B, provide genetic counseling, and potentially offer personalized treatment options. It can also help in understanding the inheritance pattern of the disorder and assessing the risk of passing it on to future generations. It is important to note that NGS genetic testing should be performed and interpreted by qualified healthcare professionals who specialize in genetics or genetic counseling. They can provide appropriate guidance and support to individuals and families undergoing genetic testing for PBD14B or any other genetic disorder.