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PRPS1 Gene Arts syndrome Genetic Test

4,400 د.إ

-21%

The PRPS1 gene is associated with Arts syndrome, a rare genetic disorder characterized by various symptoms including sensorineural hearing loss, intellectual disability, and delayed development. The condition is inherited in an X-linked recessive pattern, meaning it predominantly affects males. The PRPS1 gene plays a crucial role in the synthesis of purine nucleotides, which are essential components of DNA and RNA. Mutations in the PRPS1 gene disrupt this synthesis, leading to the symptoms observed in Arts syndrome.

To diagnose this condition, a genetic test focusing on the PRPS1 gene can be conducted. In the UAE, DNA Labs offers this specialized genetic testing service. The test is designed to identify mutations in the PRPS1 gene that are indicative of Arts syndrome. It involves collecting a DNA sample, usually through a blood draw or cheek swab, and analyzing the genetic material for specific mutations associated with the syndrome.

The cost of the PRPS1 Gene Arts syndrome Genetic Test at DNA Labs UAE is 4400 AED. This price may cover the genetic testing process, analysis, and reporting. Receiving a diagnosis through this test can be crucial for affected individuals and their families, as it provides a clear understanding of the condition and can guide treatment and management decisions. It is always recommended to consult with a healthcare professional or genetic counselor before and after undergoing genetic testing to ensure a comprehensive understanding of the test results and their implications.

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PRPS1 Gene Arts Syndrome Genetic Test

Test Details

The PRPS1 gene is associated with Arts syndrome, a rare genetic disorder that affects the nervous system and immune system. Arts syndrome is characterized by intellectual disability, early-onset deafness, optic atrophy, and recurrent infections.

NGS (Next Generation Sequencing) genetic testing can be used to identify mutations in the PRPS1 gene that are responsible for Arts syndrome. This type of testing involves sequencing the entire gene or a panel of genes associated with the disorder to identify any variations or mutations that may be present.

NGS genetic testing can provide a more comprehensive and accurate diagnosis of Arts syndrome, allowing for earlier intervention and management of symptoms. It can also help identify carriers of the gene mutation, allowing for genetic counseling and family planning.

Test Name

PRPS1 Gene Arts 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

Neurological Disorders

Doctor

Neurologist

Test Department

Genetics

Pre Test Information

Clinical History of Patient who is going for PRPS1 Gene Arts Syndrome NGS Genetic DNA Test

A Genetic Counselling session to draw a pedigree chart of family members affected with PRPS1 Gene Arts Syndrome

Test Name PRPS1 Gene Arts syndrome 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 PRPS1 Gene Arts syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with PRPS1 Gene Arts syndrome
Test Details

The PRPS1 gene is associated with Arts syndrome, a rare genetic disorder that affects the nervous system and immune system. Arts syndrome is characterized by intellectual disability, early-onset deafness, optic atrophy, and recurrent infections.

NGS (Next Generation Sequencing) genetic testing can be used to identify mutations in the PRPS1 gene that are responsible for Arts syndrome. This type of testing involves sequencing the entire gene or a panel of genes associated with the disorder to identify any variations or mutations that may be present.

NGS genetic testing can provide a more comprehensive and accurate diagnosis of Arts syndrome, allowing for earlier intervention and management of symptoms. It can also help identify carriers of the gene mutation, allowing for genetic counseling and family planning.