CERS3 Gene Ichthyosis Congenital Autosomal Recessive Type 9 Genetic Test
Welcome to DNA Labs UAE, where we offer comprehensive genetic testing services. In this blog post, we will discuss the CERS3 Gene Ichthyosis Congenital Autosomal Recessive Type 9 Genetic Test. This test is designed to diagnose a rare genetic disorder called ichthyosis, congenital, autosomal recessive, type 9.
Test Details
The CERS3 gene is associated with ichthyosis, congenital, autosomal recessive, type 9. This condition is characterized by the presence of dry, scaly skin (ichthyosis) from birth. To diagnose this disorder, our lab utilizes NGS (Next-Generation Sequencing) technology, which allows for the simultaneous analysis of multiple genes, including the CERS3 gene. NGS testing can detect various genetic variants, such as small mutations, insertions, deletions, and rearrangements in the DNA sequence.
Test Components and Price
The CERS3 Gene Ichthyosis Congenital Autosomal Recessive Type 9 Genetic Test is priced at AED 4400.0. The test requires a blood sample, extracted DNA, or one drop of blood on an FTA card.
Report Delivery
After the sample is collected, the report will be delivered within 3 to 4 weeks. Our team of experts will carefully analyze the results to provide an accurate diagnosis.
Test Type and Department
The CERS3 Gene Ichthyosis Congenital Autosomal Recessive Type 9 Genetic Test falls under the category of Osteology Dermatology Immunology Disorders. It is conducted by our experienced dermatologists in our Genetics department.
Pre Test Information
Prior to undergoing the CERS3 Gene Ichthyosis Congenital Autosomal Recessive Type 9 Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by the disorder.
Conclusion
Genetic testing, such as the CERS3 Gene Ichthyosis Congenital Autosomal Recessive Type 9 Genetic Test, plays a crucial role in confirming diagnoses and providing valuable information for genetic counseling and management of the condition. It is important to have qualified healthcare professionals, like geneticists or genetic counselors, interpret and perform these tests for accurate results.
| Test Name | CERS3 Gene Ichthyosis congenital autosomal recessive type 9 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 | Osteology Dermatology Immunology Disorders |
| Doctor | Dermatologist |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for CERS3 Gene Ichthyosis, congenital, autosomal recessive, type 9 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CERS3 Gene Ichthyosis, congenital, autosomal recessive, type 9 NGS Genetic DNA Test gene CERS3 |
| Test Details |
CERS3 gene is associated with a rare genetic disorder called ichthyosis, congenital, autosomal recessive, type 9. This condition is characterized by the presence of dry, scaly skin (ichthyosis) that is present from birth. It is inherited in an autosomal recessive manner, meaning that both copies of the CERS3 gene must be mutated for the disorder to be present. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes, including the CERS3 gene. NGS testing is a powerful tool that can detect a wide range of genetic variants, including small mutations, insertions, deletions, and rearrangements in the DNA sequence. By performing NGS genetic testing on an individual suspected of having ichthyosis, congenital, autosomal recessive, type 9, clinicians can identify mutations in the CERS3 gene. This information can help confirm the diagnosis and provide valuable information for genetic counseling and management of the condition. It is important to note that genetic testing should always be performed and interpreted by qualified healthcare professionals, such as geneticists or genetic counselors, who can provide accurate diagnosis and appropriate guidance based on the test results. |
