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BCHE Gene Butyrylcholinesterase deficiency Genetic Test Cost

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

-21%

The BCHE gene butyrylcholinesterase deficiency genetic test is a specialized diagnostic procedure aimed at identifying mutations in the BCHE gene, which is responsible for producing the enzyme butyrylcholinesterase (BChE). This enzyme plays a crucial role in the process of breaking down certain types of drugs and toxins in the body, including muscle relaxants used during surgical procedures. A deficiency in BChE can lead to prolonged paralysis or apnea after exposure to these substances, posing significant health risks during medical treatments.

The test is particularly recommended for individuals with a family history of BChE deficiency, those who have experienced unexpected reactions to anesthesia, or for those who are planning to undergo surgery and wish to ensure safe anesthesia use. By analyzing a DNA sample, usually obtained from a blood draw, the test identifies specific genetic mutations in the BCHE gene that lead to reduced activity or absence of the butyrylcholinesterase enzyme.

Conducted at DNA Labs UAE, a leading provider of genetic testing services, the test offers a comprehensive analysis with a focus on accuracy and confidentiality. The cost of the test is set at 4400 AED, reflecting the specialized nature of the testing and the expertise required to accurately interpret the results. Upon completion, the results can provide valuable information for patients and healthcare providers to make informed decisions regarding anesthesia use and to take precautions to mitigate potential risks associated with BChE deficiency.

Description

BCHE Gene Butyrylcholinesterase deficiency Genetic Test

Test Name: BCHE Gene Butyrylcholinesterase deficiency Genetic Test

Components: NGS Technology

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: Metabolic Disorders

Doctor: General Physician

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for BCHE Gene Butyrylcholinesterase deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Butyrylcholinesterase deficiency.

Test Details:

The BCHE gene encodes for the enzyme butyrylcholinesterase, which is involved in the breakdown of certain chemicals in the body, including the neurotransmitter acetylcholine. Butyrylcholinesterase deficiency is a genetic condition characterized by reduced or absent levels of this enzyme.

A Next-Generation Sequencing (NGS) genetic test is a type of genetic testing that can analyze multiple genes simultaneously. In the case of butyrylcholinesterase deficiency, an NGS genetic test can be used to identify variations or mutations in the BCHE gene that may be causing the deficiency.

This type of genetic testing can help diagnose individuals with butyrylcholinesterase deficiency and determine the specific genetic cause. It can also be used for carrier testing in individuals with a family history of the condition, as well as for prenatal testing in families at risk of having a child with the deficiency.

Overall, the BCHE gene butyrylcholinesterase deficiency NGS genetic test can provide important information about an individual’s genetic makeup and help guide medical management and treatment decisions.

Test Name	BCHE Gene Butyrylcholinesterase deficiency Genetic Test
Components
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	Metabolic Disorders
Doctor	General Physician
Test Department:	Genetics
Pre Test Information	Clinical History of Patient who is going for BCHE Gene Butyrylcholinesterase deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Butyrylcholinesterase deficiency
Test Details	The BCHE gene encodes for the enzyme butyrylcholinesterase, which is involved in the breakdown of certain chemicals in the body, including the neurotransmitter acetylcholine. Butyrylcholinesterase deficiency is a genetic condition characterized by reduced or absent levels of this enzyme. A Next-Generation Sequencing (NGS) genetic test is a type of genetic testing that can analyze multiple genes simultaneously. In the case of butyrylcholinesterase deficiency, an NGS genetic test can be used to identify variations or mutations in the BCHE gene that may be causing the deficiency. This type of genetic testing can help diagnose individuals with butyrylcholinesterase deficiency and determine the specific genetic cause. It can also be used for carrier testing in individuals with a family history of the condition, as well as for prenatal testing in families at risk of having a child with the deficiency. Overall, the BCHE gene butyrylcholinesterase deficiency NGS genetic test can provide important information about an individual’s genetic makeup and help guide medical management and treatment decisions.