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MEGF8 Gene Carpenter Syndrome Type 2 Genetic Test Cost

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

-21%

The MEGF8 Gene Carpenter Syndrome Type 2 Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to identify mutations in the MEGF8 gene that are associated with Carpenter Syndrome Type 2. This rare genetic disorder is characterized by craniosynostosis (premature fusion of skull bones), syndactyly (fusion of fingers and/or toes), obesity, and other developmental anomalies. Early and accurate diagnosis through this genetic test enables targeted management and treatment strategies, improving patient outcomes.

Priced at 4400 AED, the test involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory for the presence of specific genetic alterations in the MEGF8 gene. Results from this test can provide crucial information for affected individuals and their families regarding the condition’s prognosis, potential health risks, and the possibility of passing the gene mutation to future generations. DNA Labs UAE employs state-of-the-art technology and adheres to stringent quality controls to ensure the accuracy and reliability of the test 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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MEGF8 Gene Carpenter Syndrome Type 2 Genetic Test

Are you concerned about Carpenter syndrome type 2? DNA Labs UAE offers the MEGF8 Gene Carpenter Syndrome Type 2 Genetic Test at a cost of AED 4400.0. This test analyzes the MEGF8 gene for mutations associated with Carpenter syndrome type 2.

Test Components and Price

Price: AED 4400.0

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 MEGF8 Gene Carpenter syndrome type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MEGF8 Gene Carpenter syndrome type 2 NGS Genetic DNA Test gene MEGF8.

Test Details

The MEGF8 Gene Carpenter Syndrome Type 2 NGS Genetic Test is a type of genetic test that analyzes the MEGF8 gene for mutations associated with Carpenter syndrome type 2. Carpenter syndrome is a rare genetic disorder characterized by craniosynostosis (premature fusion of skull bones), facial abnormalities, and other developmental abnormalities.

NGS stands for Next-Generation Sequencing, which is a high-throughput sequencing technology used to analyze multiple genes simultaneously. This test uses NGS technology to sequence the MEGF8 gene and identify any genetic variations or mutations that may be present. By identifying mutations in the MEGF8 gene, this test can help diagnose Carpenter syndrome type 2 and provide important information for genetic counseling and management of the condition. It can also be used for carrier testing in individuals with a family history of the disorder.

Test Name MEGF8 Gene Carpenter syndrome type 2 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 MEGF8 Gene Carpenter syndrome type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MEGF8 Gene Carpenter syndrome type 2 NGS Genetic DNA Test gene MEGF8
Test Details

MEGF8 Gene Carpenter syndrome type 2 NGS Genetic Test is a type of genetic test that analyzes the MEGF8 gene for mutations associated with Carpenter syndrome type 2. Carpenter syndrome is a rare genetic disorder characterized by craniosynostosis (premature fusion of skull bones), facial abnormalities, and other developmental abnormalities.

NGS stands for Next-Generation Sequencing, which is a high-throughput sequencing technology used to analyze multiple genes simultaneously. This test uses NGS technology to sequence the MEGF8 gene and identify any genetic variations or mutations that may be present.

By identifying mutations in the MEGF8 gene, this test can help diagnose Carpenter syndrome type 2 and provide important information for genetic counseling and management of the condition. It can also be used for carrier testing in individuals with a family history of the disorder.

SKU: TEST-4026 Category:

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