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GLRB Gene Hyperekplexia Genetic Test Cost

Name: GLRB Gene Hyperekplexia Genetic Test Cost
SKU: TEST-1434
Price: 4400 AED
Availability: InStock

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

-21%

The GLRB gene hyperekplexia genetic test is a specialized diagnostic examination offered by DNA Labs UAE, designed to identify mutations in the GLRB gene, which are associated with hyperekplexia. Hyperekplexia, also known as startle disease, is a rare genetic disorder characterized by an exaggerated startle response to sudden stimuli, muscle stiffness, and, in severe cases, apnea and sudden infant death. This condition is primarily inherited in an autosomal dominant or recessive manner, making the identification of genetic mutations critical for diagnosis, treatment planning, and genetic counseling.

DNA Labs UAE employs cutting-edge genetic sequencing technology to analyze the GLRB gene, ensuring accurate and reliable results. The test is conducted with a simple blood sample or cheek swab, making it non-invasive and straightforward for patients. Upon completion, the results provide essential information regarding the presence of specific gene mutations, aiding in the confirmation of a hyperekplexia diagnosis and facilitating a better understanding of the condition’s potential impact on the patient and their family.

The cost of the GLRB gene hyperekplexia genetic test at DNA Labs UAE is 4400 AED. While the price may seem significant, the value of obtaining a precise diagnosis and the benefits it brings in terms of targeted treatment and family planning cannot be understated. For families and individuals facing symptoms indicative of hyperekplexia, this test represents a crucial step towards achieving clarity and taking informed actions for managing the condition.

Description

GLRB Gene Hyperekplexia Genetic Test

Components: GLRB Gene Hyperekplexia 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 GLRB Gene Hyperekplexia NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with GLRB Gene Hyperekplexia.

Test Details:

The GLRB gene is associated with a neurological disorder called hyperekplexia, also known as startle disease. Hyperekplexia is a rare genetic disorder characterized by an exaggerated startle response to unexpected stimuli, leading to muscle stiffness and temporary paralysis.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual’s genes. In the context of hyperekplexia, NGS genetic testing can be used to identify mutations or variations in the GLRB gene that may be causing the disorder. NGS testing involves sequencing large amounts of DNA in a rapid and cost-effective manner. It allows for the simultaneous analysis of multiple genes, making it particularly useful for genetic disorders with a complex or heterogeneous genetic basis, such as hyperekplexia.

By identifying specific mutations or variations in the GLRB gene through NGS testing, healthcare professionals can confirm a diagnosis of hyperekplexia and provide appropriate genetic counseling and management strategies for affected individuals and their families.

Test Name	GLRB Gene Hyperekplexia 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 GLRB Gene Hyperekplexia NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with GLRB Gene Hyperekplexia
Test Details	The GLRB gene is associated with a neurological disorder called hyperekplexia, also known as startle disease. Hyperekplexia is a rare genetic disorder characterized by an exaggerated startle response to unexpected stimuli, leading to muscle stiffness and temporary paralysis. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual’s genes. In the context of hyperekplexia, NGS genetic testing can be used to identify mutations or variations in the GLRB gene that may be causing the disorder. NGS testing involves sequencing large amounts of DNA in a rapid and cost-effective manner. It allows for the simultaneous analysis of multiple genes, making it particularly useful for genetic disorders with a complex or heterogeneous genetic basis, such as hyperekplexia. By identifying specific mutations or variations in the GLRB gene through NGS testing, healthcare professionals can confirm a diagnosis of hyperekplexia and provide appropriate genetic counseling and management strategies for affected individuals and their families.