BRAF Gene Mutations: Such as the most common mutation, V600E, which is a key biomarker in melanoma and other types of cancer. Cancer Diagnosis: Helps determine if the cancer is associated with BRAF gene mutations, enabling precise diagnosis by physicians. Guiding Treatment Options: BRAF mutations are important indicators for selecting targeted therapies, such as BRAF inhibitors, which are more effective in patients carrying these mutations. Assessing Treatment Response: The test can be used to monitor changes in mutations after starting treatment, helping evaluate patient response.

Patients with Skin Cancer (Melanoma): Especially those with advanced or metastatic stages, as BRAF gene mutations are important indicators for determining treatment options. Patients with Colon Cancer: BRAF gene mutations may indicate a poorer prognosis and affect treatment decisions. Patients with Non-Small Cell Lung Cancer: Test results can help guide appropriate treatment. Patients with Other Malignant Tumors: Such as adenocarcinomas or lymphomas, especially if there is a family history of cancer. Individuals with a Family History of Melanoma: For early assessment and potential mutation detection. Patients Showing Unexplained Symptoms: Such as tumor spread or failure to respond to conventional treatment, where BRAF testing can help identify possible causes.

New Skin Lesion Appearance: Especially if it changes in shape, color, or size. Changes in Existing Moles: Such as increased size, color change, or irregular borders. Skin Cancer Symptoms: Such as itching or bleeding from moles or skin lumps. Unexplained Weight Loss: Which may indicate cancer progression. Unexplained Tumor-Related Symptoms: Such as extreme fatigue or persistent pain in certain areas. Signs of Colon Cancer: Such as changes in bowel habits, rectal bleeding, or abdominal pain. Signs of Lung Cancer: Such as persistent cough, shortness of breath, or chest pain.

What is BRAF Test? A genetic test used to detect mutations in the BRAF gene, which is associated with certain types of cancer, such as skin cancer and colon cancer. When is this test recommended? It is recommended at the diagnosis of skin cancer, or when there is suspicion of colon cancer or any other cancers linked to the BRAF gene. How is the test performed? A blood or tissue sample is collected and analyzed in the laboratory using genetic techniques to detect mutations. Does the test require any preparations? Usually, no special preparations are needed, but it is recommended to inform the doctor about any medications or supplements being taken. How long does it take to get results? Results usually take several days to a week, depending on the laboratory and testing procedures. Is the test painful? Blood draw or tissue sampling may cause some discomfort, but it is not considered highly painful. What are the normal levels for the BRAF gene? There are no "normal levels" for this test; it determines whether a mutation is present in the gene or not. What do the test results mean? A positive result indicates the presence of a BRAF gene mutation, which can affect treatment options. A negative result means no known mutations are detected. Can cancer be treated based on test results? Yes, if a BRAF mutation is present, targeted therapies such as BRAF inhibitors may be recommended for more effective treatment. Can this test be used in research? Yes, BRAF testing is used in research to study the relationship between mutations and various aspects of cancer, including treatment response.

Positive Result: Indicates the presence of a mutation in the BRAF gene, such as the V600E mutation, which is an important biomarker in certain cancers like melanoma and colon cancer. Negative Result: Indicates that no known mutations in the BRAF gene are detected, suggesting the patient does not carry mutations associated with specific cancers.

BRAF Gene Mutation Test in KSA | Lahalak Platform

An advanced genetic test to detect BRAF gene mutations associated with certain cancers, aiding in early diagnosis and determining the most appropriate and precise treatment plan.

Prices starts from: 760.32 SAR

Scientific name: BRAF Gene Mutation Test

BRAF analysis (BRAF gene analysis) is a genetic test used to detect mutations in the BRAF gene, which is considered one of the important genes involved in cell growth signaling pathways. This analysis helps diagnose certain types of cancer, especially skin cancer (melanoma), and can also be used in other cancers such as colorectal and lung cancer....

Service type Genetic test (Blood)

Duration 10-15 minutes

Fasting Fasting is not required

Prices Starting from 760.32 SAR

Included Services

BRAF Test
The optimal health guidance based on the result.
Personal support services from Lahalak

Medical Service Information

Purpose Test

BRAF Gene Mutations: Such as the most common mutation, V600E, which is a key biomarker in melanoma and other types of cancer.
Cancer Diagnosis: Helps determine if the cancer is associated with BRAF gene mutations, enabling precise diagnosis by physicians.
Guiding Treatment Options: BRAF mutations are important indicators for selecting targeted therapies, such as BRAF inhibitors, which are more effective in patients carrying these mutations.
Assessing Treatment Response: The test can be used to monitor changes in mutations after starting treatment, helping evaluate patient response.

Recommended groups

Patients with Skin Cancer (Melanoma): Especially those with advanced or metastatic stages, as BRAF gene mutations are important indicators for determining treatment options.
Patients with Colon Cancer: BRAF gene mutations may indicate a poorer prognosis and affect treatment decisions.
Patients with Non-Small Cell Lung Cancer: Test results can help guide appropriate treatment.
Patients with Other Malignant Tumors: Such as adenocarcinomas or lymphomas, especially if there is a family history of cancer.
Individuals with a Family History of Melanoma: For early assessment and potential mutation detection.
Patients Showing Unexplained Symptoms: Such as tumor spread or failure to respond to conventional treatment, where BRAF testing can help identify possible causes.

Symptoms indicative

New Skin Lesion Appearance: Especially if it changes in shape, color, or size.
Changes in Existing Moles: Such as increased size, color change, or irregular borders.
Skin Cancer Symptoms: Such as itching or bleeding from moles or skin lumps.
Unexplained Weight Loss: Which may indicate cancer progression.
Unexplained Tumor-Related Symptoms: Such as extreme fatigue or persistent pain in certain areas.
Signs of Colon Cancer: Such as changes in bowel habits, rectal bleeding, or abdominal pain.

FAQs

What is BRAF Test? A genetic test used to detect mutations in the BRAF gene, which is associated with certain types of cancer, such as skin cancer and colon cancer.
When is this test recommended? It is recommended at the diagnosis of skin cancer, or when there is suspicion of colon cancer or any other cancers linked to the BRAF gene.
How is the test performed? A blood or tissue sample is collected and analyzed in the laboratory using genetic techniques to detect mutations.
Does the test require any preparations? Usually, no special preparations are needed, but it is recommended to inform the doctor about any medications or supplements being taken.
How long does it take to get results? Results usually take several days to a week, depending on the laboratory and testing procedures.
Is the test painful? Blood draw or tissue sampling may cause some discomfort, but it is not considered highly painful.

Normal Levels

Positive Result: Indicates the presence of a mutation in the BRAF gene, such as the V600E mutation, which is an important biomarker in certain cancers like melanoma and colon cancer.
Negative Result: Indicates that no known mutations in the BRAF gene are detected, suggesting the patient does not carry mutations associated with specific cancers.