SMC3 Gene Cornelia de Lange syndrome type 3 Genetic Test
At DNA Labs UAE, we offer the SMC3 Gene Cornelia de Lange syndrome type 3 Genetic Test. This test is designed to identify any variants or mutations in the SMC3 gene that may be associated with Cornelia de Lange syndrome type 3 (CdLS3). CdLS3 is a genetic disorder that affects various parts of the body and is characterized by distinctive facial features, growth delays, intellectual disability, and limb abnormalities.
Test Components and Price
The SMC3 Gene Cornelia de Lange syndrome type 3 Genetic Test is priced at 4400.0 AED. The test requires a sample of either blood, extracted DNA, or one drop of blood on an FTA card.
Report Delivery
Once the sample is received, the report will be delivered within 3 to 4 weeks.
Method and Test Type
The SMC3 Gene Cornelia de Lange syndrome type 3 Genetic Test utilizes Next-Generation Sequencing (NGS) technology. NGS is a high-throughput DNA sequencing technology that allows for the rapid sequencing of large amounts of DNA. This enables the identification of genetic variants and mutations associated with various diseases and conditions, including CdLS3. The test falls under the category of Osteology Dermatology Immunology Disorders.
Doctor and Test Department
The SMC3 Gene Cornelia de Lange syndrome type 3 Genetic Test is conducted by a Dermatologist in our Genetics department.
Pre Test Information
Prior to undergoing the SMC3 Gene Cornelia de Lange syndrome type 3 Genetic Test, it is important to provide the clinical history of the patient. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected by CdLS3 and the SMC3 gene.
Test Details
The SMC3 gene is specifically associated with Cornelia de Lange syndrome type 3 (CdLS3). CdLS3 is a genetic disorder that affects multiple parts of the body and is characterized by distinctive facial features, growth delays, intellectual disability, and limb abnormalities. By sequencing the SMC3 gene using NGS technology, this test can identify any variants or mutations that may be present, aiding in the confirmation of a CdLS3 diagnosis in individuals with suspected symptoms. It can also be used for carrier testing in families with a known history of the condition.
Please note that genetic testing for CdLS3 should always be performed by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate counseling and support.
| Test Name | SMC3 Gene Cornelia de Lange syndrome type 3 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 SMC3 Gene Cornelia de Lange syndrome type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SMC3 Gene Cornelia de Lange syndrome type 3 NGS Genetic DNA Test gene SMC3 |
| Test Details |
The SMC3 gene is a gene that is associated with Cornelia de Lange syndrome type 3 (CdLS3). Cornelia de Lange syndrome is a genetic disorder that affects many parts of the body and is characterized by distinctive facial features, growth delays, intellectual disability, and limb abnormalities. NGS stands for Next-Generation Sequencing, which is a high-throughput DNA sequencing technology. NGS allows for the rapid sequencing of large amounts of DNA, which can be used to identify genetic variants and mutations associated with various diseases and conditions, including CdLS3. A genetic test for CdLS3 using NGS technology would involve sequencing the SMC3 gene to identify any variants or mutations that may be present. This can help confirm a diagnosis of CdLS3 in individuals with suspected symptoms and can also be used for carrier testing in families with a known history of the condition. It is important to note that genetic testing for CdLS3 should be performed by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate counseling and support. |
