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ABCD3 Gene Bile acid synthesis defect type 5 congenital Genetic Test

Name: ABCD3 Gene Bile acid synthesis defect type 5 congenital Genetic Test
SKU: TEST-2189
Price: 4400 AED
Availability: InStock

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

-21%

The ABCD3 Gene Bile Acid Synthesis Defect Type 5 is a rare genetic disorder that disrupts the body’s ability to properly produce and process bile acids. These acids are essential for the digestion and absorption of fats and fat-soluble vitamins. Mutations in the ABCD3 gene lead to this condition, which can result in a range of symptoms from mild to severe, including liver dysfunction, fat malabsorption, and vitamin deficiencies.

To diagnose this condition, a specific genetic test can be conducted to identify mutations in the ABCD3 gene. This test is crucial for confirming the diagnosis, understanding the severity of the condition, and guiding treatment decisions. It involves analyzing the patient’s DNA to look for specific alterations associated with the disorder.

In the United Arab Emirates, this genetic test is available at DNA Labs UAE, a leading provider of genetic testing services. The cost of the test is 4400 AED. DNA Labs UAE utilizes state-of-the-art technology to ensure accurate and reliable results, providing essential information for patients and their families dealing with Bile Acid Synthesis Defect Type 5. Early diagnosis and intervention can significantly improve the quality of life for individuals affected by this condition.

Description

ABCD3 Gene Bile Acid Synthesis Defect Type 5 Congenital Genetic Test

Test Name: ABCD3 Gene Bile Acid Synthesis Defect Type 5 Congenital Genetic Test

Components: Price: 4400.0 AED

Sample Condition: Blood

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 ABCD3 Gene Bile Acid Synthesis Defect Type 5, congenital NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Bile Acid Synthesis Defect Type 5, congenital.

Test Details: The ABCD3 gene is involved in the synthesis of bile acids, which are important for the digestion and absorption of dietary fats. A defect in the ABCD3 gene can lead to a condition called bile acid synthesis defect type 5, which is a congenital disorder.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the analysis of multiple genes simultaneously. It involves sequencing the DNA or RNA of an individual to identify any variations or mutations in the genes being tested.

In the case of bile acid synthesis defect type 5, NGS genetic testing can be used to identify any mutations or variations in the ABCD3 gene that may be causing the condition. By identifying the specific genetic variant causing the defect, NGS genetic testing can help in confirming a diagnosis, providing information about the inheritance pattern, and guiding appropriate management and treatment options for individuals with bile acid synthesis defect type 5.

Test Name	ABCD3 Gene Bile acid synthesis defect type 5 congenital Genetic Test
Components
Price	4400.0 AED
Sample Condition	Blood
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 ABCD3 Gene Bile acid synthesis defect type 5, congenital NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Bile acid synthesis defect type 5, congenital
Test Details	The ABCD3 gene is involved in the synthesis of bile acids, which are important for the digestion and absorption of dietary fats. A defect in the ABCD3 gene can lead to a condition called bile acid synthesis defect type 5, which is a congenital disorder. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the analysis of multiple genes simultaneously. It involves sequencing the DNA or RNA of an individual to identify any variations or mutations in the genes being tested. In the case of bile acid synthesis defect type 5, NGS genetic testing can be used to identify any mutations or variations in the ABCD3 gene that may be causing the condition. By identifying the specific genetic variant causing the defect, NGS genetic testing can help in confirming a diagnosis, providing information about the inheritance pattern, and guiding appropriate management and treatment options for individuals with bile acid synthesis defect type 5.