CEP63 Gene Microcephaly CEP63 related Genetic Test
Test Name: CEP63 Gene Microcephaly CEP63 related Genetic Test
Components: Blood or Extracted DNA or One drop Blood on FTA Card
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: Dysmorphology
Doctor: Pediatrics
Test Department: Genetics
Pre Test Information: Clinical History of Patient who is going for CEP63 Gene Microcephaly, CEP63 related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CEP63 Gene Microcephaly, CEP63 related NGS Genetic DNA Test gene CEP63
Test Details: CEP63 gene microcephaly is a rare genetic disorder characterized by the development of an abnormally small head and brain size (microcephaly). It is caused by mutations in the CEP63 gene, which provides instructions for making a protein involved in cell division and DNA repair.
CEP63-related NGS genetic testing is a diagnostic test that uses next-generation sequencing (NGS) technology to analyze the CEP63 gene for mutations or variations. This test can identify specific changes in the gene that may be responsible for microcephaly or other related conditions.
NGS genetic testing involves sequencing the DNA of an individual to identify any variations or mutations in specific genes. In the case of CEP63-related NGS genetic testing, the CEP63 gene is analyzed to determine if there are any changes that may be linked to microcephaly. This type of genetic testing can help confirm a diagnosis of CEP63 gene microcephaly and provide valuable information about the specific genetic cause of the condition.
It can also help guide treatment decisions, provide information about the risk of the condition in other family members, and assist in genetic counseling.
It’s important to note that CEP63-related NGS genetic testing is typically performed by healthcare professionals specializing in genetics and genetic testing. The results of the test should be interpreted by a qualified healthcare provider who can provide appropriate counseling and guidance based on the individual’s specific situation.
Test Name | CEP63 Gene Microcephaly CEP63 related 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 | Dysmorphology |
Doctor | Pediatrics |
Test Department: | Genetics |
Pre Test Information | Clinical History of Patient who is going for CEP63 Gene Microcephaly, CEP63 related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CEP63 Gene Microcephaly, CEP63 related NGS Genetic DNA Test gene CEP63 |
Test Details |
CEP63 gene microcephaly is a rare genetic disorder characterized by the development of an abnormally small head and brain size (microcephaly). It is caused by mutations in the CEP63 gene, which provides instructions for making a protein involved in cell division and DNA repair. CEP63-related NGS genetic testing is a diagnostic test that uses next-generation sequencing (NGS) technology to analyze the CEP63 gene for mutations or variations. This test can identify specific changes in the gene that may be responsible for microcephaly or other related conditions. NGS genetic testing involves sequencing the DNA of an individual to identify any variations or mutations in specific genes. In the case of CEP63-related NGS genetic testing, the CEP63 gene is analyzed to determine if there are any changes that may be linked to microcephaly. This type of genetic testing can help confirm a diagnosis of CEP63 gene microcephaly and provide valuable information about the specific genetic cause of the condition. It can also help guide treatment decisions, provide information about the risk of the condition in other family members, and assist in genetic counseling. It’s important to note that CEP63-related NGS genetic testing is typically performed by healthcare professionals specializing in genetics and genetic testing. The results of the test should be interpreted by a qualified healthcare provider who can provide appropriate counseling and guidance based on the individual’s specific situation. |