RAB3GAP2 Gene Warburg micro syndrome type 2 Genetic Test
At DNA Labs UAE, we offer the RAB3GAP2 Gene Warburg micro syndrome type 2 Genetic Test. This test helps in diagnosing and understanding the rare genetic disorder known as Warburg micro syndrome type 2. The test is performed using Next-Generation Sequencing (NGS) technology, which allows for the simultaneous analysis of multiple genes.
Test Details
The RAB3GAP2 gene is associated with Warburg micro syndrome type 2. This syndrome is characterized by intellectual disability, developmental delay, microcephaly (small head size), vision problems, and movement disorders. The syndrome is inherited in an autosomal recessive manner, meaning that both parents must carry a mutated copy of the RAB3GAP2 gene for their child to develop the disorder.
NGS genetic testing is a powerful tool that can identify mutations or variants in the RAB3GAP2 gene, providing a confirmed diagnosis and information about the specific genetic variant(s) present in an individual. This information can help healthcare providers better understand the underlying cause of the individual’s symptoms and guide treatment and management options.
Test Components and Price
- Components: RAB3GAP2 Gene Warburg micro syndrome type 2 Genetic Test
- Price: 4400.0 AED
Sample Condition
The test can be performed using blood or extracted DNA. Alternatively, a single drop of blood can be collected on an FTA Card for testing.
Report Delivery
The test results will be delivered within 3 to 4 weeks.
Test Method
The RAB3GAP2 Gene Warburg micro syndrome type 2 Genetic Test is performed using NGS technology.
Test Type
The test falls under the category of Dysmorphology.
Referring Doctor and Test Department
The test is recommended for Pediatrics and falls under the Genetics department.
Pre Test Information
Prior to the test, it is important to provide the clinical history of the patient who is going for the RAB3GAP2 Gene Warburg micro syndrome type 2 NGS Genetic DNA Test. Additionally, a genetic counseling session is advised to draw a pedigree chart of family members affected by the disorder.
Genetic counseling and support from healthcare professionals or genetic counselors are crucial throughout the testing process.
At DNA Labs UAE, we are committed to providing accurate and reliable genetic testing services. Our RAB3GAP2 Gene Warburg micro syndrome type 2 Genetic Test can help in the diagnosis and management of this rare genetic disorder. For more information or to schedule a test, please contact us.
| Test Name | RAB3GAP2 Gene Warburg micro syndrome type 2 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 RAB3GAP2 Gene Warburg micro syndrome type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with RAB3GAP2 Gene Warburg micro syndrome type 2 NGS Genetic DNA Test gene RAB3GAP2 |
| Test Details |
The RAB3GAP2 gene is associated with a rare genetic disorder called Warburg micro syndrome type 2. This syndrome is characterized by multiple abnormalities including intellectual disability, developmental delay, small head size (microcephaly), vision problems, and movement disorders. It is inherited in an autosomal recessive manner, meaning that an individual must inherit two copies of the mutated gene (one from each parent) to develop the syndrome. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes. In the context of Warburg micro syndrome type 2, NGS testing can be used to identify mutations or variants in the RAB3GAP2 gene that may be responsible for the disorder. This testing can help confirm a diagnosis and provide information about the specific genetic variant(s) present in an individual. NGS genetic testing typically involves obtaining a DNA sample (usually through a blood sample or saliva sample) from the individual being tested. The DNA is then sequenced using advanced technology to identify any variations or mutations in the RAB3GAP2 gene. The results of the test can help healthcare providers better understand the underlying genetic cause of the individual’s symptoms and may inform treatment and management options. It is important to note that genetic testing, including NGS testing, should be done under the guidance of a healthcare professional or genetic counselor who can provide appropriate counseling and support. |
