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PITX2 Gene Axenfeld-Rieger Syndrome Type 1 Genetic Test Cost

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

-21%

The PITX2 Gene Axenfeld-Rieger Syndrome Type 1 Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, aimed at identifying mutations in the PITX2 gene, which are associated with Axenfeld-Rieger Syndrome Type 1 (ARS1). Axenfeld-Rieger Syndrome is a rare genetic disorder characterized by abnormalities in the development of the eyes, teeth, and abdominal region, potentially leading to glaucoma and vision loss. The PITX2 gene plays a crucial role in the early development of these structures, and mutations in this gene can disrupt normal development, leading to the manifestations of ARS1.

The test involves collecting a DNA sample, usually through a blood draw or cheek swab, and analyzing it for specific mutations in the PITX2 gene. It is a critical tool for genetic counseling, early diagnosis, and management of the syndrome, allowing for targeted interventions to mitigate some of the complications associated with the condition.

The cost of the PITX2 Gene Axenfeld-Rieger Syndrome Type 1 Genetic Test at DNA Labs UAE is 4400 AED. This investment covers the comprehensive analysis required to detect the presence of the genetic mutation, offering invaluable information for affected individuals and their families. Through this testing, families can gain a better understanding of the condition, its potential impact, and the genetic risks for future offspring, thereby facilitating informed decisions about health and family planning.

Description

PITX2 Gene Axenfeld-Rieger syndrome type 1 Genetic Test

Test Name: PITX2 Gene Axenfeld-Rieger syndrome type 1 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: Dysmorphology

Doctor: Pediatrics

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for PITX2 Gene Axenfeld-Rieger syndrome type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PITX2 Gene Axenfeld-Rieger syndrome type 1 NGS Genetic DNA Test gene PITX2

Test Details:

The PITX2 gene is associated with Axenfeld-Rieger syndrome type 1, a rare genetic disorder that affects the development of the eyes, teeth, and other parts of the body. NGS (Next-Generation Sequencing) is a high-throughput DNA sequencing technology that allows for the rapid sequencing of large amounts of genetic material. In the context of genetic testing for Axenfeld-Rieger syndrome type 1, NGS can be used to analyze the PITX2 gene for any mutations or variations that may be associated with the condition.

A NGS genetic test for Axenfeld-Rieger syndrome type 1 would involve collecting a sample of DNA, typically through a blood sample or saliva sample, from the individual being tested. The DNA would then be sequenced using NGS technology to identify any potential mutations or variations in the PITX2 gene. The results of the test can help confirm a diagnosis of Axenfeld-Rieger syndrome type 1 and provide information about the specific genetic changes involved.

It is important to note that genetic testing for Axenfeld-Rieger syndrome type 1 should be performed by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate genetic counseling and support.

Test Name	PITX2 Gene Axenfeld-Rieger syndrome type 1 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	Dysmorphology
Doctor	Pediatrics
Test Department:	Genetics
Pre Test Information	Clinical History of Patient who is going for PITX2 Gene Axenfeld-Rieger syndrome type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PITX2 Gene Axenfeld-Rieger syndrome type 1 NGS Genetic DNA Test gene PITX2
Test Details	The PITX2 gene is associated with Axenfeld-Rieger syndrome type 1, a rare genetic disorder that affects the development of the eyes, teeth, and other parts of the body. NGS (Next-Generation Sequencing) is a high-throughput DNA sequencing technology that allows for the rapid sequencing of large amounts of genetic material. In the context of genetic testing for Axenfeld-Rieger syndrome type 1, NGS can be used to analyze the PITX2 gene for any mutations or variations that may be associated with the condition. A NGS genetic test for Axenfeld-Rieger syndrome type 1 would involve collecting a sample of DNA, typically through a blood sample or saliva sample, from the individual being tested. The DNA would then be sequenced using NGS technology to identify any potential mutations or variations in the PITX2 gene. The results of the test can help confirm a diagnosis of Axenfeld-Rieger syndrome type 1 and provide information about the specific genetic changes involved. It is important to note that genetic testing for Axenfeld-Rieger syndrome type 1 should be performed by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate genetic counseling and support.