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TBX1 Gene DiGeorge Syndrome Genetic Test Cost

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

-21%

The TBX1 Gene DiGeorge Syndrome Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to detect mutations in the TBX1 gene, which are strongly associated with DiGeorge Syndrome (22q11.2 deletion syndrome). This syndrome is a disorder characterized by a spectrum of clinical features, including congenital heart defects, distinct facial characteristics, immune deficiencies, and developmental delays. The test is crucial for early diagnosis and management of the condition, allowing for timely interventions and support for affected individuals.

At DNA Labs UAE, the TBX1 Gene DiGeorge Syndrome Genetic Test is conducted using advanced genomic technologies to ensure accurate and reliable results. The test is priced at 4400 AED, reflecting the sophisticated nature of the genetic analysis and the comprehensive insights it provides into the patient’s condition. By opting for this test, patients and their families can gain valuable information on the genetic basis of DiGeorge Syndrome, facilitating informed decisions about care and treatment strategies.

Description

TBX1 Gene DiGeorge Syndrome Genetic Test

At DNA Labs UAE, we offer the TBX1 Gene DiGeorge Syndrome Genetic Test to help diagnose individuals with DiGeorge syndrome. This genetic disorder is characterized by the incomplete development of certain tissues and organs, and is typically caused by a deletion of a small piece of chromosome 22 that includes the TBX1 gene.

Our TBX1 Gene DiGeorge Syndrome Genetic Test is conducted using Next-generation sequencing (NGS) technology. NGS allows for the rapid and cost-effective sequencing of large amounts of DNA, making it an efficient method for identifying genetic variations associated with DiGeorge syndrome.

The cost of the TBX1 Gene DiGeorge Syndrome Genetic Test is AED 4400.0. We accept blood or extracted DNA samples, as well as one drop of blood on an FTA card. The test report will be delivered within 3 to 4 weeks.

Our test is performed by our expert team of genetics professionals in the Pediatrics department. Prior to the test, we recommend a Genetic Counselling session to gather clinical history and draw a pedigree chart of family members affected by DiGeorge syndrome. This information helps us provide accurate and personalized results.

By analyzing the sequence of the TBX1 gene, our healthcare professionals can identify any genetic variations or mutations that may be associated with DiGeorge syndrome. This information is crucial for confirming a diagnosis, providing genetic counseling, and guiding treatment options for individuals with DiGeorge syndrome.

If you suspect that you or a loved one may have DiGeorge syndrome, we encourage you to consider our TBX1 Gene DiGeorge Syndrome Genetic Test. Contact DNA Labs UAE today to schedule an appointment and take a step towards understanding your genetic health.

Test Name	TBX1 Gene DiGeorge syndrome 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 TBX1 Gene DiGeorge syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TBX1 Gene DiGeorge syndrome NGS Genetic DNA Test gene TBX1
Test Details	The TBX1 gene is associated with DiGeorge syndrome, a genetic disorder characterized by the incomplete development of certain tissues and organs. DiGeorge syndrome is typically caused by a deletion of a small piece of chromosome 22, which includes the TBX1 gene. Next-generation sequencing (NGS) is a genetic testing method that allows for the rapid and cost-effective sequencing of large amounts of DNA. NGS can be used to identify genetic variations, including deletions or mutations in the TBX1 gene, which can help diagnose DiGeorge syndrome. By performing an NGS genetic test, healthcare professionals can analyze the sequence of the TBX1 gene and determine if there are any genetic variations that may be associated with DiGeorge syndrome. This information can be used to confirm a diagnosis, provide genetic counseling, and guide treatment options for individuals with DiGeorge syndrome.