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AAAS Gene Achalasia addisonianism alacrimia syndrome Genetic Test

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

-21%

The AAAS Gene Achalasia-Addisonianism-Alacrimia Syndrome Genetic Test is a specialized diagnostic examination offered by DNA Labs UAE. This test is designed to detect mutations in the AAAS gene, which are implicated in the rare, autosomal recessive disorder known as Triple-A Syndrome (Achalasia-Addisonianism-Alacrimia Syndrome). Patients with this condition often exhibit a range of symptoms including esophageal achalasia, adrenal gland insufficiency (Addison’s disease), and a decreased production of tears (alacrimia).

Given the complex nature of this syndrome and its significant impact on an individual’s health, accurate diagnosis is crucial for appropriate management and treatment. The genetic test offered by DNA Labs UAE utilizes advanced molecular techniques to analyze the AAAS gene for any mutations that are known to cause the syndrome, providing a precise diagnosis that can guide treatment decisions and genetic counseling.

The cost of the AAAS Gene Achalasia-Addisonianism-Alacrimia Syndrome Genetic Test at DNA Labs UAE is 4400 AED. This price reflects the sophisticated technology and expertise required to accurately identify mutations in the AAAS gene. By opting for this test, patients and their families can gain valuable insights into their genetic health, enabling them to take proactive steps in managing the condition and improving their quality of life.

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AAAS Gene Achalasia addisonianism alacrimia syndrome Genetic Test

At DNA Labs UAE, we offer the AAAS Gene Achalasia addisonianism alacrimia syndrome Genetic Test at a cost of AED 4400.0.

Test Components

  • Price: 4400.0 AED
  • Sample Condition: Blood
  • Report Delivery: 3 to 4 Weeks
  • Method: NGS Technology
  • Test Type: Neurological Disorders
  • Doctor: Neurologist
  • Test Department: Genetics

Pre Test Information

Before undergoing the AAAS Gene Achalasia addisonianism alacrimia syndrome Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by the syndrome.

Test Details

The AAAS gene is associated with a rare genetic disorder known as Achalasia-Addisonianism-Alacrimia syndrome (AAA syndrome). This syndrome is characterized by difficulty swallowing (achalasia), adrenal gland dysfunction (addisonianism), and a lack of tears (alacrimia).

The NGS (Next Generation Sequencing) Genetic Test is a type of genetic testing that utilizes advanced sequencing technologies to rapidly sequence millions of DNA strands simultaneously. This enables the identification of genetic variations, including mutations in the AAAS gene that may cause AAA syndrome. NGS testing can be utilized for diagnosis, risk assessment, and personalized treatment options for individuals with genetic disorders.

Test Name AAAS Gene Achalasia addisonianism alacrimia syndrome Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Neurological Disorders
Doctor Neurologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for AAAS Gene Achalasia addisonianism alacrimia syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with AAAS Gene Achalasia addisonianism alacrimia syndrome
Test Details

The AAAS gene is associated with a rare genetic disorder called Achalasia-Addisonianism-Alacrimia syndrome (AAA syndrome). This syndrome is characterized by difficulty swallowing (achalasia), adrenal gland dysfunction (addisonianism), and a lack of tears (alacrimia).

NGS (Next Generation Sequencing) Genetic Test is a type of genetic testing that uses advanced sequencing technologies to rapidly sequence millions of DNA strands at once. This allows for the identification of genetic variations, including mutations in the AAAS gene that may cause AAA syndrome. NGS testing can be used for diagnosis, risk assessment, and personalized treatment options for individuals with genetic disorders.

SKU: TEST-1011 Category:

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