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AR Gene Spinal and Bulbar Muscular Atrophy X-Linked Genetic Test Cost

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

-21%

The AR Gene Spinal and Bulbar Muscular Atrophy X-Linked Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to detect mutations in the AR gene, which are responsible for Spinal and Bulbar Muscular Atrophy (SBMA), also known as Kennedy’s disease. This condition is an X-linked recessive disorder, meaning it predominantly affects males, though females can be carriers. SBMA is characterized by the degeneration of motor neurons in the spinal cord and brainstem, leading to muscle weakness and atrophy, as well as bulbar involvement that affects speech and swallowing.

The test involves analyzing the patient’s DNA to identify specific mutations in the androgen receptor (AR) gene, which plays a crucial role in the development and maintenance of male characteristics. Mutations in this gene lead to the abnormal expansion of a CAG trinucleotide repeat, causing the neurological and muscular symptoms associated with SBMA.

Offered at a cost of 4400 AED, this genetic test is a critical tool for confirming the diagnosis of SBMA, enabling early intervention and management of the condition. It also provides essential information for family planning, as it can help identify carriers of the mutation who may be at risk of passing the condition to their offspring. Conducted at the state-of-the-art facilities of DNA Labs UAE, this test is a cornerstone in the personalized approach to genetic disorders, offering hope and support to affected individuals and their families.

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AR Gene Spinal and Bulbar Muscular Atrophy X-Linked Genetic Test

Welcome to DNA Labs UAE, where we offer the AR Gene Spinal and Bulbar Muscular Atrophy X-Linked Genetic Test. This test is designed to diagnose spinal and bulbar muscular atrophy (SBMA), also known as Kennedy’s disease.

Test Components and Cost

  • Test Name: AR Gene Spinal and Bulbar Muscular Atrophy X-Linked Genetic Test
  • Price: 4400.0 AED

Sample Condition

The test can be conducted using a blood sample, extracted DNA, or one drop of blood on an FTA card.

Report Delivery

Once the sample is received, the report will be delivered within 3 to 4 weeks.

Method

The test utilizes Next-Generation Sequencing (NGS) technology.

Test Type

The AR Gene Spinal and Bulbar Muscular Atrophy X-Linked Genetic Test is specifically designed for neurological disorders.

Doctor and Test Department

This test is conducted by a neurologist in the Genetics department.

Pre Test Information

Prior to the test, a clinical history of the patient is taken. Additionally, a genetic counseling session is conducted to draw a pedigree chart of family members affected by AR Gene Spinal and Bulbar Muscular Atrophy X-Linked.

Test Details

The AR Gene Spinal and Bulbar Muscular Atrophy X-Linked Genetic Test is a comprehensive genetic test used to diagnose SBMA. SBMA is a rare genetic disorder primarily affecting males and is caused by mutations in the AR gene on the X chromosome.

The test analyzes the entire coding region of the AR gene, along with other relevant genes, using NGS technology. This allows for the identification of genetic variations or mutations associated with SBMA, providing a comprehensive analysis of the disease’s genetic factors.

The test is typically performed using a blood or saliva sample, and results are usually available within a few weeks. A positive result confirms the presence of an AR gene mutation, confirming a diagnosis of SBMA.

Genetic testing for SBMA is beneficial for individuals experiencing symptoms of the disease and those with a family history of SBMA. It helps confirm a diagnosis, provides information about disease progression and prognosis, and assists in reproductive decisions and genetic counseling.

It is important to note that this test is specific to SBMA and does not screen for other genetic disorders or conditions. It is typically ordered by a healthcare provider specializing in genetics or neurology and may require pre-authorization from insurance companies due to its specialized nature.

Test Name AR Gene Spinal and bulbar muscular atrophy X-linked Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card o
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 AR Gene Spinal and bulbar muscular atrophy X-linked NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with AR Gene Spinal and bulbar muscular atrophy X-linked
Test Details

AR Gene Spinal and bulbar muscular atrophy X-linked NGS Genetic Test is a genetic test that is used to diagnose spinal and bulbar muscular atrophy (SBMA), also known as Kennedy’s disease. SBMA is a rare genetic disorder that primarily affects males and is caused by mutations in the AR gene on the X chromosome.

The test utilizes next-generation sequencing (NGS) technology to analyze the entire coding region of the AR gene, as well as other relevant genes, to identify any genetic variations or mutations that may be associated with SBMA. This allows for a comprehensive analysis of the genetic factors contributing to the disease.

The test is typically performed on a blood sample or a saliva sample, and the results are usually available within a few weeks. A positive result indicates the presence of a mutation in the AR gene, confirming a diagnosis of SBMA.

Genetic testing for SBMA can be useful for individuals who are experiencing symptoms of the disease, as well as for individuals with a family history of SBMA. It can help to confirm a diagnosis, provide information about disease progression and prognosis, and inform reproductive decisions and genetic counseling.

It is important to note that this test is specific to SBMA and does not screen for other genetic disorders or conditions. Additionally, it is typically ordered by a healthcare provider who specializes in genetics or neurology, and it may require pre-authorization from insurance companies due to its specialized nature.

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