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RELN Gene Epilepsy familial temporal lobe type 7 Genetic Test

4,400 د.إ

-21%

The RELN Gene Epilepsy Familial Temporal Lobe Type 7 Genetic Test is a specialized diagnostic examination offered by DNA Labs UAE, designed to identify mutations in the RELN gene that are associated with Familial Temporal Lobe Epilepsy Type 7 (FTLE7). This condition is a form of epilepsy characterized by seizures originating in the temporal lobes of the brain, which can affect behavior, memory, and emotional control. The test aims to provide crucial genetic information that can aid in the precise diagnosis, management, and treatment planning for individuals and families affected by this condition. The cost of the test is set at 4400 AED, reflecting the comprehensive analysis and the detailed insights it offers into the genetic underpinnings of FTLE7. This test is particularly valuable for families with a history of temporal lobe epilepsy, offering them a clearer understanding of their genetic risk and potential preventive measures or targeted therapies.

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RELN Gene Epilepsy familial temporal lobe type 7 Genetic Test

Test Name: RELN Gene Epilepsy familial temporal lobe type 7 Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

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: Neurological Disorders

Doctor: Neurologist

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for RELN Gene Epilepsy, familial temporal lobe type 7 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with RELN Gene Epilepsy, familial temporal lobe type 7.

Test Details: The RELN gene is associated with a form of epilepsy known as familial temporal lobe epilepsy (FTLE). FTLE is a type of epilepsy that runs in families and is characterized by seizures that originate in the temporal lobe of the brain. The RELN gene provides instructions for making a protein called reelin, which plays a role in the development and function of the brain.

NGS (next-generation sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to rapidly sequence large amounts of DNA. NGS can be used to identify mutations or variations in the RELN gene that may be associated with FTLE. If a person has a family history of FTLE or is experiencing symptoms of the condition, a genetic test may be recommended.

The test involves collecting a sample of the person’s DNA, usually through a blood sample, and sequencing the RELN gene to look for any mutations or variations. If a mutation or variation is identified, it can help confirm a diagnosis of FTLE and provide information about the inheritance pattern of the condition within the family. This information can be used to help guide treatment and management of the condition.

Test Name RELN Gene Epilepsy familial temporal lobe type 7 Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card o
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Neurological Disorders
Doctor Neurologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for RELN Gene Epilepsy, familial temporal lobe type 7 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with RELN Gene Epilepsy, familial temporal lobe type 7
Test Details

The RELN gene is associated with a form of epilepsy known as familial temporal lobe epilepsy (FTLE). FTLE is a type of epilepsy that runs in families and is characterized by seizures that originate in the temporal lobe of the brain. The RELN gene provides instructions for making a protein called reelin, which plays a role in the development and function of the brain.

NGS (next-generation sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to rapidly sequence large amounts of DNA. NGS can be used to identify mutations or variations in the RELN gene that may be associated with FTLE.

If a person has a family history of FTLE or is experiencing symptoms of the condition, a genetic test may be recommended. The test involves collecting a sample of the person’s DNA, usually through a blood sample, and sequencing the RELN gene to look for any mutations or variations.

If a mutation or variation is identified, it can help confirm a diagnosis of FTLE and provide information about the inheritance pattern of the condition within the family. This information can be used to help guide treatment and management of the condition.