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BRAF Gene Cardiofaciocutaneous Syndrome Genetic Test Cost

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

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The BRAF Gene Cardiofaciocutaneous Syndrome Genetic Test is a specialized diagnostic procedure designed to identify mutations in the BRAF gene, which are known to cause Cardiofaciocutaneous (CFC) syndrome. CFC syndrome is a rare genetic condition that affects various parts of the body, including the heart, facial features, and skin. Symptoms may include heart defects, developmental delays, distinctive facial characteristics, and skin abnormalities.

This test is conducted at DNA Labs UAE, a leading facility in genetic testing and analysis. The test involves collecting a DNA sample, typically through a blood draw or cheek swab, and examining it for specific mutations in the BRAF gene that are associated with CFC syndrome. This genetic test is crucial for confirming a diagnosis of CFC syndrome, which can enable appropriate management and treatment plans for the affected individuals.

The cost of the BRAF Gene Cardiofaciocutaneous Syndrome Genetic Test at DNA Labs UAE is 4400 AED. This investment in genetic testing can provide vital information for affected families, aiding in understanding the condition, planning for medical care, and accessing support services. It’s important for potential patients or their guardians to consult with a healthcare provider or a genetic counselor to discuss the benefits, limitations, and implications of this test.

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  • This test is not intended for medical diagnosis or treatment
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BRAF Gene Cardiofaciocutaneous Syndrome Genetic Test

At DNA Labs UAE, we offer the BRAF Gene Cardiofaciocutaneous Syndrome Genetic Test. This test helps in diagnosing Cardiofaciocutaneous syndrome (CFC syndrome) by analyzing mutations in the BRAF gene and other relevant genes associated with this rare genetic disorder.

Test Components

  • Test Name: BRAF Gene Cardiofaciocutaneous Syndrome Genetic Test
  • 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: Cardiovascular Pneumology Disorders
  • Doctor: Cardiologist
  • Test Department: Genetics

Pre Test Information

Prior to undergoing the BRAF Gene Cardiofaciocutaneous 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 CFC syndrome. This will help in identifying the presence of the BRAF gene mutation in the family.

Test Details

The BRAF gene is responsible for producing a protein called B-Raf, which plays a crucial role in regulating cell growth and division. Mutations in the BRAF gene can lead to various genetic disorders, including Cardiofaciocutaneous syndrome. This rare genetic disorder is characterized by abnormalities in the heart, facial features, and skin.

Individuals with CFC syndrome may exhibit distinctive facial features, heart defects, skin abnormalities, intellectual disability, and delayed development. To diagnose CFC syndrome, Next-Generation Sequencing (NGS) genetic testing is employed. NGS testing utilizes advanced sequencing technologies to efficiently analyze multiple genes simultaneously, including the BRAF gene.

NGS testing helps confirm a diagnosis of CFC syndrome and enables appropriate medical management and genetic counseling for affected individuals and their families.

Test Name BRAF Gene Cardiofaciocutaneous 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 Cardiovascular Pneumology Disorders
Doctor Cardiologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for BRAF Gene Cardiofaciocutaneous syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with BRAF Gene Cardiofaciocutaneous syndrome NGS Genetic DNA Test gene BRAF
Test Details

The BRAF gene is a gene that provides instructions for making a protein called B-Raf. This protein is involved in signaling pathways that regulate cell growth and division. Mutations in the BRAF gene can lead to various genetic disorders, including Cardiofaciocutaneous syndrome (CFC syndrome).

Cardiofaciocutaneous syndrome is a rare genetic disorder characterized by abnormalities in the heart (cardio-), facial features (facio-), and skin (cutaneous). It is caused by mutations in multiple genes, including the BRAF gene. Individuals with CFC syndrome may have distinctive facial features, heart defects, skin abnormalities, intellectual disability, and delayed development.

Next-generation sequencing (NGS) genetic testing is a type of genetic testing that uses advanced sequencing technologies to rapidly and efficiently analyze multiple genes simultaneously. It allows for the identification of specific mutations or changes in the DNA sequence of the BRAF gene and other relevant genes associated with CFC syndrome. NGS testing can help confirm a diagnosis of CFC syndrome and guide appropriate medical management and genetic counseling for affected individuals and their families.

SKU: TEST-3351 Category:

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