EFTUD2 Gene Mandibulofacial dysostosis with microcephaly Genetic Test
Cost: 4400.0 AED
Test Components:
- 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 EFTUD2 Gene Mandibulofacial dysostosis with microcephaly NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with EFTUD2 Gene Mandibulofacial dysostosis with microcephaly.
Test Details:
The EFTUD2 gene is associated with a condition called Mandibulofacial dysostosis with microcephaly (MFDM). This condition is characterized by abnormal development of the facial bones and structures, as well as a small head size (microcephaly).
NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that can analyze multiple genes simultaneously. It is a powerful tool for identifying genetic mutations or variations that may be responsible for a particular condition. In the case of MFDM, NGS genetic testing can be used to detect mutations or variations in the EFTUD2 gene that may be causing the disorder. By identifying the specific genetic cause of MFDM, NGS genetic testing can help with diagnosis, provide information about the prognosis, and assist in genetic counseling for affected individuals and their families. It can also potentially guide treatment options or management strategies for individuals with this condition.
Test Name | EFTUD2 Gene Mandibulofacial dysostosis with microcephaly Genetic Test |
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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 EFTUD2 Gene Mandibulofacial dysostosis with microcephaly NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with EFTUD2 Gene Mandibulofacial dysostosis with microcephaly |
Test Details | The EFTUD2 gene is associated with a condition called Mandibulofacial dysostosis with microcephaly (MFDM). This condition is characterized by abnormal development of the facial bones and structures, as well as a small head size (microcephaly). NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that can analyze multiple genes simultaneously. It is a powerful tool for identifying genetic mutations or variations that may be responsible for a particular condition. In the case of MFDM, NGS genetic testing can be used to detect mutations or variations in the EFTUD2 gene that may be causing the disorder. By identifying the specific genetic cause of MFDM, NGS genetic testing can help with diagnosis, provide information about the prognosis, and assist in genetic counseling for affected individuals and their families. It can also potentially guide treatment options or management strategies for individuals with this condition. |