Sale!

BRAF Gene LEOPARD Syndrome Type 3 Genetic Test Cost

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

-21%

The BRAF Gene LEOPARD Syndrome Type 3 Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, aimed at identifying mutations in the BRAF gene, which are associated with LEOPARD Syndrome Type 3. This condition is a rare genetic disorder characterized by multiple congenital anomalies, including skin abnormalities, heart defects, and distinctive facial features. The test is crucial for individuals suspected of having the syndrome or for those with a family history of the condition, as it aids in confirming the diagnosis, guiding treatment decisions, and assessing the risk of passing the condition to offspring. The test cost is set at 4400 AED, reflecting the comprehensive analysis and expertise required to accurately identify the presence of BRAF gene mutations. DNA Labs UAE employs state-of-the-art genetic testing technologies to ensure reliable and precise results, supporting patients and healthcare providers in managing the condition effectively.

Description

BRAF Gene LEOPARD syndrome type 3 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 BRAF Gene LEOPARD syndrome type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with BRAF Gene LEOPARD syndrome type 3 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 cell signaling pathways that regulate cell growth and division. LEOPARD syndrome, also known as Noonan syndrome with multiple lentigines, is a rare genetic disorder that affects various parts of the body, including the skin, heart, and eyes. It is caused by mutations in several different genes, including the BRAF gene.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technology to analyze multiple genes simultaneously. It can detect mutations or variations in the DNA sequence of genes, including the BRAF gene, associated with LEOPARD syndrome.

By performing an NGS genetic test for LEOPARD syndrome, healthcare professionals can identify specific mutations in the BRAF gene that may be causing the disorder. This information can help in making a definitive diagnosis, providing appropriate medical management, and offering genetic counseling to affected individuals and their families.

Test Name	BRAF Gene LEOPARD syndrome type 3 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 BRAF Gene LEOPARD syndrome type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with BRAF Gene LEOPARD syndrome type 3 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 cell signaling pathways that regulate cell growth and division. LEOPARD syndrome, also known as Noonan syndrome with multiple lentigines, is a rare genetic disorder that affects various parts of the body, including the skin, heart, and eyes. It is caused by mutations in several different genes, including the BRAF gene. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technology to analyze multiple genes simultaneously. It can detect mutations or variations in the DNA sequence of genes, including the BRAF gene, associated with LEOPARD syndrome. By performing an NGS genetic test for LEOPARD syndrome, healthcare professionals can identify specific mutations in the BRAF gene that may be causing the disorder. This information can help in making a definitive diagnosis, providing appropriate medical management, and offering genetic counseling to affected individuals and their families.