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EFNB1 Gene Craniofrontonasal Syndrome Genetic Test Cost

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

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The EFNB1 Gene Craniofrontonasal Syndrome Genetic Test is a specialized diagnostic assessment offered by DNA Labs UAE, aimed at identifying mutations in the EFNB1 gene, which are linked to Craniofrontonasal Syndrome (CFNS). CFNS is a rare genetic disorder characterized by distinctive craniofacial, skeletal, and dermatological abnormalities, often manifesting differently between males and females due to its X-linked inheritance pattern. The condition is primarily caused by mutations in the EFNB1 gene, which plays a crucial role in cell signaling and tissue development during embryonic growth.

This genetic test is crucial for families with a history of CFNS, offering them an opportunity for early diagnosis, which is essential for the management and treatment of the condition. The process involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory for any abnormalities in the EFNB1 gene.

At DNA Labs UAE, the EFNB1 Gene Craniofrontonasal Syndrome Genetic Test is available for 4,400 AED. The test is conducted with a high level of accuracy and confidentiality, ensuring that individuals and families receive precise information about their genetic health. Results from this test can guide healthcare professionals in creating a tailored management plan for those affected by CFNS, potentially improving their quality of life and mitigating some of the condition’s more severe manifestations.

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  • This test is not intended for medical diagnosis or treatment
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EFNB1 Gene Craniofrontonasal syndrome Genetic Test

At DNA Labs UAE, we offer the EFNB1 Gene Craniofrontonasal syndrome Genetic Test at a cost of AED 4400.0. This test is used to diagnose the craniofrontonasal syndrome, a condition that affects the development of the head and face.

Test Components and Price

The EFNB1 Gene Craniofrontonasal syndrome Genetic Test includes the following 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: Dysmorphology
  • Doctor: Pediatrics
  • Test Department: Genetics

The cost of the test is AED 4400.0.

Pre Test Information

Before undergoing the EFNB1 Gene Craniofrontonasal syndrome Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by the syndrome.

Test Details

The EFNB1 gene is associated with craniofrontonasal syndrome, a condition that primarily affects the development of the head and face. It is more commonly seen in females due to its X-linked inheritance pattern.

NGS (Next-Generation Sequencing) genetic testing is used to analyze multiple genes simultaneously. In the case of craniofrontonasal syndrome, NGS is used to analyze the EFNB1 gene for any mutations or variations. By identifying genetic changes in the EFNB1 gene, this test can confirm a diagnosis of craniofrontonasal syndrome and provide information about the specific genetic variant causing the condition.

This information is crucial in determining the prognosis, planning appropriate medical management, and providing genetic counseling to affected individuals and their families.

Test Name EFNB1 Gene Craniofrontonasal syndrome 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 EFNB1 Gene Craniofrontonasal syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with EFNB1 Gene Craniofrontonasal syndrome NGS Genetic DNA Test gene EFNB1
Test Details

The EFNB1 gene is associated with a condition called craniofrontonasal syndrome. This syndrome primarily affects the development of the head and face, leading to various craniofacial abnormalities. It is an X-linked genetic disorder, meaning it is more commonly seen in females than males.

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 craniofrontonasal syndrome, NGS can be used to analyze the EFNB1 gene for any mutations or variations that may be present.

By identifying any genetic changes in the EFNB1 gene, NGS genetic testing can help confirm a diagnosis of craniofrontonasal syndrome and provide information about the specific genetic variant causing the condition. This information can be useful in determining the prognosis, planning appropriate medical management, and providing genetic counseling to affected individuals and their families.

SKU: TEST-4074 Category:

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