CROCC Gene Neurodevelopmental Disorder: Symptoms, Diagnosis, and Genetic Testing
Welcome to DNA Labs UAE, your trusted genetic testing laboratory. In this blog post, we will discuss the CROCC gene, its role in neurodevelopmental disorders, and the genetic test available to diagnose this condition. Read on to learn more about the symptoms, diagnosis process, and the cost of the CROCC gene-related genetic test.
Test Name: CROCC Gene Neurodevelopmental Disorder
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
Before undergoing the CROCC Gene Neurodevelopmental Disorder test, it is important to provide the clinical history of the patient. A genetic counseling session will also be conducted to draw a pedigree chart of family members affected by CROCC Gene Neurodevelopmental Disorder.
Test Details
The CROCC gene, also known as the ciliary rootlet coiled-coil protein, is crucial for the development and function of cilia. Cilia are hair-like structures found on the surface of cells that play important roles in cell signaling and movement.
Individuals with mutations in the CROCC gene may experience a neurodevelopmental disorder characterized by intellectual disability, autism spectrum disorder, and various physical abnormalities.
To diagnose a CROCC gene-related neurodevelopmental disorder, a Next-Generation Sequencing (NGS) genetic test is performed. NGS is a high-throughput sequencing technology that allows for the rapid sequencing of multiple genes simultaneously.
The genetic test involves collecting a sample of DNA, typically through a blood sample or saliva sample, from the individual suspected of having the disorder. The DNA is then sequenced using NGS technology, and the resulting data is analyzed to identify any mutations or variations in the CROCC gene.
The results of the genetic test provide valuable information for diagnosis, prognosis, and potential treatment options for individuals with a CROCC gene-related neurodevelopmental disorder. It also aids in genetic counseling and family planning for affected individuals and families.
It is crucial to note that genetic testing should always be done under the guidance of a healthcare professional or genetic counselor who can provide appropriate counseling and support throughout the testing process.
Conclusion
The CROCC gene-related neurodevelopmental disorder is a complex condition that can have significant impacts on an individual’s life. The availability of the CROCC Gene Neurodevelopmental Disorder genetic test at DNA Labs UAE provides an opportunity for accurate diagnosis and personalized treatment plans.
If you suspect that you or a loved one may have a CROCC gene-related neurodevelopmental disorder, we encourage you to consult with a neurologist or genetic counselor to discuss the possibility of undergoing this genetic test. Early diagnosis and intervention can make a significant difference in managing the condition and improving quality of life.
For more information about the CROCC Gene Neurodevelopmental Disorder genetic test or to schedule an appointment, please contact DNA Labs UAE. Our team of experts is here to support you every step of the way.
| Test Name | CROCC Gene Neurodevelopmental disorder CROCC related 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 CROCC Gene Neurodevelopmental disorder, CROCC related NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with CROCC Gene Neurodevelopmental disorder, CROCC related |
| Test Details |
The CROCC gene, also known as the ciliary rootlet coiled-coil protein, is involved in the development and function of cilia. Cilia are hair-like structures found on the surface of cells that play important roles in cell signaling and movement. Mutations in the CROCC gene have been associated with a neurodevelopmental disorder characterized by intellectual disability, autism spectrum disorder, and various physical abnormalities. To diagnose a CROCC gene-related neurodevelopmental disorder, a Next-Generation Sequencing (NGS) genetic test can be performed. NGS is a high-throughput sequencing technology that allows for the rapid sequencing of multiple genes simultaneously. This type of genetic testing can identify mutations or variations in the CROCC gene that may be responsible for the neurodevelopmental disorder. The NGS genetic test typically involves collecting a sample of DNA, usually through a blood sample or saliva sample, from the individual suspected of having the disorder. The DNA is then sequenced using NGS technology, and the resulting data is analyzed to identify any mutations or variations in the CROCC gene. The results of the genetic test can provide valuable information for diagnosis, prognosis, and potential treatment options for individuals with a CROCC gene-related neurodevelopmental disorder. It can also help in genetic counseling and family planning for individuals and families affected by the disorder. It is important to note that genetic testing should be done under the guidance of a healthcare professional or genetic counselor who can provide appropriate counseling and support throughout the testing process. |
