Genetic changes: Identifying mutations or alterations in the DNA sequence of a set of genes associated with specific diseases. Genetic disorders: Detecting genetic factors that may lead to hereditary disorders or increase the risk of certain diseases. Cancers: Identifying genetic mutations linked to various types of cancer, which helps in diagnosing the condition and guiding treatment options. Personalized treatment information: Providing data on the potential response to treatment based on an individual’s genetic makeup.

Individuals with a family history of genetic diseases: Those who have relatives affected by certain genetic conditions. Patients with unexplained symptoms: Such as persistent symptoms without a clear diagnosis. Individuals at high risk for cancer: Based on family history or specific risk factors. People seeking personalized treatment: Those who wish to know their treatment options based on their genetic makeup. Patients involved in clinical research: Individuals participating in studies related to genetic disorders or cancers.

Unexplained symptoms: Such as chronic diseases or conditions with unknown causes. Family history of genetic diseases: Like recurrent cancers or other hereditary disorders. Abnormalities in routine test results: Such as unusual findings in blood tests or medical examinations. Symptoms related to cancer: Such as unexplained weight loss, unexplained pain, or changes in eating habits. Recurring health disorders: Such as heart problems, endocrine disorders, or neurological issues.

What is the purpose of this test? The goal is to identify genetic changes linked to specific diseases to assist in diagnosis and provide personalized treatment options. How is the test performed? A sample of blood or tissue is collected and then analyzed using advanced sequencing techniques. Does the patient need special preparations before the test? Typically, no special preparations are required, but it is advisable to consult the doctor about any specific precautions. What is the expected time to receive results? Results usually take from several days to weeks, depending on the laboratory. How are the test results interpreted? Results are interpreted by specialized doctors who compare the detected mutations with known values to understand health risks. What are the risks associated with the test? The test is generally safe, but minor complications may occur during sample collection. What do positive results mean? They may indicate the presence of genetic mutations that could lead to certain diseases, requiring further evaluation and appropriate treatment.

Negative results: Indicate no mutations or significant genetic changes, which is considered the normal or baseline condition. Positive results: Indicate the presence of mutations or genetic changes that may be associated with certain health risks.

Targeted Multi-Gene Sequencing | Lahalak Platform

Advanced genetic analysis of specific gene groups associated with certain diseases, facilitating accurate diagnosis of hereditary disorders and cancers to guide treatment.

Prices starts from: 5653.03 SAR

Scientific name: Targeted Multi-Gene Panel Sequencing

Targeted Sequencing - Multi Gene Panel is an advanced test used to examine a group of genes associated with specific diseases. This analysis allows for the identification of genetic variations or mutations in several genes simultaneously, facilitating the diagnosis of genetic disorders and cancers. This technique is especially used in personalized...

Targeted Multi-Gene Panel Sequencing - Targeted Multi-Gene Panel

Service type Advanced Genetic Test

Duration 15-20 minutes

Fasting Fasting is not required

Prices Starting from 5653.03 SAR

Included Services

Targeted Sequencing - Multi Gene Panel Test
The optimal health guidance based on the result.
Personal support services from Lahalak

Medical Service Information

Purpose Test

Genetic changes: Identifying mutations or alterations in the DNA sequence of a set of genes associated with specific diseases.
Genetic disorders: Detecting genetic factors that may lead to hereditary disorders or increase the risk of certain diseases.
Cancers: Identifying genetic mutations linked to various types of cancer, which helps in diagnosing the condition and guiding treatment options.
Personalized treatment information: Providing data on the potential response to treatment based on an individual’s genetic makeup.

Recommended groups

Individuals with a family history of genetic diseases: Those who have relatives affected by certain genetic conditions.
Patients with unexplained symptoms: Such as persistent symptoms without a clear diagnosis.
Individuals at high risk for cancer: Based on family history or specific risk factors.
People seeking personalized treatment: Those who wish to know their treatment options based on their genetic makeup.
Patients involved in clinical research: Individuals participating in studies related to genetic disorders or cancers.

Symptoms indicative

Unexplained symptoms: Such as chronic diseases or conditions with unknown causes.
Family history of genetic diseases: Like recurrent cancers or other hereditary disorders.
Abnormalities in routine test results: Such as unusual findings in blood tests or medical examinations.
Symptoms related to cancer: Such as unexplained weight loss, unexplained pain, or changes in eating habits.
Recurring health disorders: Such as heart problems, endocrine disorders, or neurological issues.

FAQs

What is the purpose of this test? The goal is to identify genetic changes linked to specific diseases to assist in diagnosis and provide personalized treatment options.
How is the test performed? A sample of blood or tissue is collected and then analyzed using advanced sequencing techniques.
Does the patient need special preparations before the test? Typically, no special preparations are required, but it is advisable to consult the doctor about any specific precautions.
What is the expected time to receive results? Results usually take from several days to weeks, depending on the laboratory.
How are the test results interpreted? Results are interpreted by specialized doctors who compare the detected mutations with known values to understand health risks.
What are the risks associated with the test? The test is generally safe, but minor complications may occur during sample collection.

Normal Levels

Negative results: Indicate no mutations or significant genetic changes, which is considered the normal or baseline condition.
Positive results: Indicate the presence of mutations or genetic changes that may be associated with certain health risks.

Conditions & Notices

The terms and conditions announced on the "Lahalak" medical platform apply.
There are no special conditions for the service other than those mentioned.

Targeted Multi-Gene Sequencing | Lahalak Platform

Included Services

Medical Service Information

Purpose Test

Recommended groups

Symptoms indicative

FAQs

Normal Levels

Conditions & Notices

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