Sale!

GATA6 Gene Pancreatic agenesis and congenital heart defects Genetic Test Cost

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

-21%

The “GATA6 Gene Pancreatic Agenesis and Congenital Heart Defects Genetic Test” is a specialized diagnostic tool offered by DNA Labs UAE, designed to detect mutations in the GATA6 gene. Mutations in this gene are known to cause pancreatic agenesis, a rare condition where the pancreas fails to develop properly, leading to diabetes and related issues from birth. Additionally, these mutations can result in various congenital heart defects, which are structural problems with the heart present from birth. The test is crucial for early diagnosis and management of these conditions, providing essential information for personalized treatment plans and family planning. The cost of the test is 4400 AED, making it a valuable investment for families with a history of these genetic conditions, offering them peace of mind and the ability to make informed health decisions.

Description

GATA6 Gene Pancreatic Agenesis and Congenital Heart Defects Genetic Test

Test Name: GATA6 Gene Pancreatic Agenesis and Congenital Heart Defects Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

Price: 4400.0 AED

Report Delivery: 3 to 4 Weeks

Method: NGS Technology

Test Type: Cardiovascular Pneumology Disorders

Doctor: Cardiologist

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for GATA6 Gene Pancreatic Agenesis and Congenital Heart Defects NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with GATA6 Gene Pancreatic Agenesis and Congenital Heart Defects NGS Genetic DNA Test gene GATA6

Test Details: The GATA6 gene is a transcription factor that plays a crucial role in the development of various organs, including the pancreas and the heart. Mutations in the GATA6 gene have been associated with pancreatic agenesis, which is the absence or underdevelopment of the pancreas, and congenital heart defects. NGS (Next-Generation Sequencing) genetic testing is a technique that allows for the simultaneous sequencing of multiple genes or even the entire genome. It is commonly used in clinical settings to identify genetic variations and mutations associated with specific diseases or conditions. In the context of GATA6 gene-related disorders, NGS genetic testing can be used to analyze the entire coding region of the GATA6 gene to identify any pathogenic mutations or variants. This can help in diagnosing individuals with pancreatic agenesis and congenital heart defects, as well as providing valuable information for genetic counseling and management of these conditions. NGS genetic testing has revolutionized the field of genetics by enabling faster, more comprehensive, and cost-effective analysis of genetic variations. It has greatly improved our ability to identify disease-causing mutations and understand the genetic basis of various disorders, including those related to the GATA6 gene.

Test Name	GATA6 Gene Pancreatic agenesis and congenital heart defects 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	Cardiovascular Pneumology Disorders
Doctor	Cardiologist
Test Department:	Genetics
Pre Test Information	Clinical History of Patient who is going for GATA6 Gene Pancreatic agenesis and congenital heart defects NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with GATA6 Gene Pancreatic agenesis and congenital heart defects NGS Genetic DNA Test gene GATA6
Test Details	The GATA6 gene is a transcription factor that plays a crucial role in the development of various organs, including the pancreas and the heart. Mutations in the GATA6 gene have been associated with pancreatic agenesis, which is the absence or underdevelopment of the pancreas, and congenital heart defects. NGS (Next-Generation Sequencing) genetic testing is a technique that allows for the simultaneous sequencing of multiple genes or even the entire genome. It is commonly used in clinical settings to identify genetic variations and mutations associated with specific diseases or conditions. In the context of GATA6 gene-related disorders, NGS genetic testing can be used to analyze the entire coding region of the GATA6 gene to identify any pathogenic mutations or variants. This can help in diagnosing individuals with pancreatic agenesis and congenital heart defects, as well as providing valuable information for genetic counseling and management of these conditions. NGS genetic testing has revolutionized the field of genetics by enabling faster, more comprehensive, and cost-effective analysis of genetic variations. It has greatly improved our ability to identify disease-causing mutations and understand the genetic basis of various disorders, including those related to the GATA6 gene.