RAD21 Gene Cornelia de Lange syndrome type 4 Genetic Test
Test Name: RAD21 Gene Cornelia de Lange syndrome type 4 Genetic Test
Components: RAD21 Gene
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 RAD21 Gene Cornelia de Lange syndrome type 4 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with RAD21 Gene Cornelia de Lange syndrome type 4 NGS Genetic DNA Test gene RAD21
Test Details:
The RAD21 gene is one of the genes associated with Cornelia de Lange syndrome (CdLS), specifically type 4. CdLS is a rare genetic disorder that affects multiple body systems and causes developmental delays and distinctive facial features. NGS (Next-Generation Sequencing) genetic testing refers to a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously.
In the context of CdLS, NGS testing can be used to identify mutations or variations in the RAD21 gene that may be responsible for causing CdLS type 4. NGS genetic testing for CdLS involves collecting a sample of DNA, typically through a blood sample or saliva sample, from the individual suspected of having CdLS. The DNA is then sequenced using NGS technology to identify any mutations or variations in the RAD21 gene.
The results of the NGS genetic test can help confirm a diagnosis of CdLS type 4 and provide information about the specific genetic variant involved. This information can be useful for understanding the underlying cause of the disorder, predicting the prognosis, and guiding treatment and management strategies.
It is important to note that genetic testing for CdLS, including NGS testing, should be done under the guidance of a healthcare professional or genetic counselor who specializes in genetic disorders. They can help interpret the results and provide appropriate genetic counseling and support.
Test Name | RAD21 Gene Cornelia de Lange syndrome type 4 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 RAD21 Gene Cornelia de Lange syndrome type 4 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with RAD21 Gene Cornelia de Lange syndrome type 4 NGS Genetic DNA Test gene RAD21 |
Test Details |
The RAD21 gene is one of the genes associated with Cornelia de Lange syndrome (CdLS), specifically type 4. CdLS is a rare genetic disorder that affects multiple body systems and causes developmental delays and distinctive facial features. NGS (Next-Generation Sequencing) genetic testing refers to a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the context of CdLS, NGS testing can be used to identify mutations or variations in the RAD21 gene that may be responsible for causing CdLS type 4. NGS genetic testing for CdLS involves collecting a sample of DNA, typically through a blood sample or saliva sample, from the individual suspected of having CdLS. The DNA is then sequenced using NGS technology to identify any mutations or variations in the RAD21 gene. The results of the NGS genetic test can help confirm a diagnosis of CdLS type 4 and provide information about the specific genetic variant involved. This information can be useful for understanding the underlying cause of the disorder, predicting the prognosis, and guiding treatment and management strategies. It is important to note that genetic testing for CdLS, including NGS testing, should be done under the guidance of a healthcare professional or genetic counselor who specializes in genetic disorders. They can help interpret the results and provide appropriate genetic counseling and support. |