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RAB3GAP1 Gene Warburg Micro Syndrome Type 1 Genetic Test Cost

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

-21%

The RAB3GAP1 gene is essential in the regulation of a process known as membrane trafficking within cells. Mutations in this gene are primarily associated with Warburg Micro Syndrome Type 1, a rare genetic disorder characterized by a range of symptoms including developmental delays, microcephaly, eye abnormalities, and hypotonia. The condition is inherited in an autosomal recessive manner, meaning that an individual must inherit two copies of the mutated gene, one from each parent, to be affected.

To diagnose this syndrome and identify the specific genetic mutation, a genetic test targeting the RAB3GAP1 gene can be conducted. This test is crucial for families seeking a definitive diagnosis, understanding the risk of recurrence in future pregnancies, and accessing appropriate care and support for affected individuals.

DNA Labs UAE offers this specialized genetic test for Warburg Micro Syndrome Type 1. The test involves analyzing the patient’s DNA to detect mutations in the RAB3GAP1 gene that are indicative of the syndrome. This process provides a precise diagnosis, enabling targeted management and care for the affected individual.

The cost of the RAB3GAP1 Gene Warburg Micro Syndrome Type 1 Genetic Test at DNA Labs UAE is 4400 AED. This price includes the full analysis and reporting, offering families valuable insights into their genetic makeup and aiding in the management of the condition. It’s important for interested individuals to consult with healthcare professionals and genetic counselors to understand the implications of the test results fully.

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RAB3GAP1 Gene Warburg micro 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

Neurological Disorders

Doctor

Neurologist

Test Department

Genetics

Pre Test Information

Clinical History of Patient who is going for RAB3GAP1 Gene Warburg micro syndrome type 1 NGS Genetic DNA Test

A Genetic Counselling session to draw a pedigree chart of family members affected with RAB3GAP1 Gene Warburg micro syndrome type 1

Test Details

The RAB3GAP1 gene is responsible for producing a protein that plays a role in the development and function of the brain and other tissues. Mutations in this gene can lead to a rare genetic disorder known as Warburg micro syndrome type 1.

Warburg micro syndrome type 1 is characterized by a variety of symptoms, including intellectual disability, developmental delay, small head size (microcephaly), vision problems, and movement disorders. Individuals with this condition may also have structural abnormalities of the brain and eyes, as well as other health issues such as seizures and hearing loss.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously, allowing for a comprehensive assessment of an individual’s genetic makeup. In the case of Warburg micro syndrome type 1, NGS testing can be used to identify mutations in the RAB3GAP1 gene that may be causing the condition.

By identifying the specific genetic mutation causing Warburg micro syndrome type 1, NGS testing can provide a definitive diagnosis for individuals with suspected or confirmed symptoms of the disorder. This information can be valuable for guiding medical management and providing appropriate genetic counseling for affected individuals and their families.

Test Name RAB3GAP1 Gene Warburg micro syndrome type 1 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 RAB3GAP1 Gene Warburg micro syndrome type 1 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with RAB3GAP1 Gene Warburg micro syndrome type 1
Test Details

The RAB3GAP1 gene is responsible for producing a protein that plays a role in the development and function of the brain and other tissues. Mutations in this gene can lead to a rare genetic disorder known as Warburg micro syndrome type 1.

Warburg micro syndrome type 1 is characterized by a variety of symptoms, including intellectual disability, developmental delay, small head size (microcephaly), vision problems, and movement disorders. Individuals with this condition may also have structural abnormalities of the brain and eyes, as well as other health issues such as seizures and hearing loss.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously, allowing for a comprehensive assessment of an individual’s genetic makeup. In the case of Warburg micro syndrome type 1, NGS testing can be used to identify mutations in the RAB3GAP1 gene that may be causing the condition.

By identifying the specific genetic mutation causing Warburg micro syndrome type 1, NGS testing can provide a definitive diagnosis for individuals with suspected or confirmed symptoms of the disorder. This information can be valuable for guiding medical management and providing appropriate genetic counseling for affected individuals and their families.

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