PQBP1 Gene Renpenning syndrome Genetic Test
Components: PQBP1 Gene Renpenning syndrome Genetic Test
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: Clinical History of Patient who is going for PQBP1 Gene Renpenning syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PQBP1 Gene Renpenning syndrome.
Test Details: The PQBP1 gene is associated with Renpenning syndrome, which is a rare genetic disorder characterized by intellectual disability, speech and language impairments, and certain physical features. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of Renpenning syndrome, NGS genetic testing can be used to identify mutations or variations in the PQBP1 gene that may be responsible for the disorder. NGS genetic testing for Renpenning syndrome involves obtaining a DNA sample from the individual being tested, usually through a blood sample or cheek swab. The DNA is then sequenced using NGS technology to analyze the entire coding region of the PQBP1 gene. The results of the NGS genetic test can provide information about any mutations or variations in the PQBP1 gene that may be present in the individual being tested. This information can help confirm a diagnosis of Renpenning syndrome and provide valuable information for genetic counseling and family planning.
Test Name | PQBP1 Gene Renpenning syndrome 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 PQBP1 Gene Renpenning syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with PQBP1 Gene Renpenning syndrome |
Test Details |
The PQBP1 gene is associated with Renpenning syndrome, which is a rare genetic disorder characterized by intellectual disability, speech and language impairments, and certain physical features. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of Renpenning syndrome, NGS genetic testing can be used to identify mutations or variations in the PQBP1 gene that may be responsible for the disorder. NGS genetic testing for Renpenning syndrome involves obtaining a DNA sample from the individual being tested, usually through a blood sample or cheek swab. The DNA is then sequenced using NGS technology to analyze the entire coding region of the PQBP1 gene. The results of the NGS genetic test can provide information about any mutations or variations in the PQBP1 gene that may be present in the individual being tested. This information can help confirm a diagnosis of Renpenning syndrome and provide valuable information for genetic counseling and family planning. |