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EFTUD2 Gene Mandibulofacial dysostosis with microcephaly Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The EFTUD2 Gene Mandibulofacial Dysostosis with Microcephaly Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the EFTUD2 gene, which are linked to the rare genetic disorder known as Mandibulofacial Dysostosis with Microcephaly (MFDM). This condition is characterized by distinctive craniofacial features, microcephaly, and often other physical and developmental abnormalities. The test is crucial for accurate diagnosis, guiding treatment options, and providing essential information for genetic counseling.

Performed through a detailed analysis of the patient’s DNA, this test seeks to detect specific genetic alterations in the EFTUD2 gene that are responsible for the development of MFDM. Early diagnosis through genetic testing can significantly benefit affected individuals and their families by enabling timely intervention and support services.

The cost of the EFTUD2 Gene Mandibulofacial Dysostosis with Microcephaly Genetic Test at DNA Labs UAE is 4400 AED. This investment covers the comprehensive process of collecting a DNA sample, usually through a blood draw or cheek swab, conducting the genetic analysis, and providing a detailed report on the findings. The test is conducted with high precision and confidentiality, ensuring patients receive accurate and actionable results.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
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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
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.

SKU: TEST-1551