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SCARB2 Gene Epilepsy progressive myoclonic type 4 with or without renal failure Genetic Test

4,400 د.إ

-21%

The SCARB2 Gene Epilepsy Progressive Myoclonic Type 4 with or without Renal Failure Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the SCARB2 gene. This gene is crucial for understanding a rare form of epilepsy known as Progressive Myoclonic Epilepsy Type 4 (EPM4), which may also be associated with renal failure in some cases. The condition is characterized by progressive muscle jerks, seizures, and, in some instances, kidney dysfunction. Identifying mutations in the SCARB2 gene can help in confirming the diagnosis, allowing for a better-informed approach to treatment and management of the condition.

The test is priced at 4400 AED and involves analyzing the patient’s DNA to detect any genetic abnormalities that could be responsible for the condition. By opting for this test at DNA Labs UAE, patients and healthcare providers can gain crucial insights into the genetic underpinnings of the disease, paving the way for personalized treatment plans and interventions. This genetic test is an essential tool for those suspected of having this form of epilepsy, offering hope for improved quality of life through targeted therapies and management strategies.

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SCARB2 Gene Epilepsy progressive myoclonic type 4 with or without renal failure Genetic Test

Welcome to DNA Labs UAE, where we offer the SCARB2 Gene Epilepsy progressive myoclonic type 4 with or without renal failure Genetic Test. This test helps diagnose a rare genetic disorder associated with the SCARB2 gene. Read on to learn more about the test components, price, sample condition, report delivery, method, test type, referring doctor, test department, pre-test information, and test details.

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

Neurological Disorders

Referring Doctor

Neurologist

Test Department

Genetics

Pre Test Information

Before undergoing the SCARB2 Gene Epilepsy progressive myoclonic type 4 with or without renal failure Genetic Test, it is important to provide the clinical history of the patient. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected with SCARB2 Gene Epilepsy, progressive myoclonic type 4, with or without renal failure.

Test Details

The SCARB2 gene is associated with a rare genetic disorder called epilepsy, progressive myoclonic type 4, with or without renal failure. This disorder is characterized by seizures, muscle twitches or jerks (myoclonus), and progressive neurological decline. In some cases, it may also lead to kidney failure.

NGS genetic testing for this disorder involves sequencing the SCARB2 gene to identify any genetic mutations that may be causing the condition. This test can help diagnose the disorder and provide information about the severity of the condition and the risk of kidney failure. It can also help identify carriers of the genetic mutation, which can be useful for family planning.

Treatment for this disorder typically involves managing symptoms with anticonvulsant medications and supportive care.

Test Name SCARB2 Gene Epilepsy progressive myoclonic type 4 with or without renal failure 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 SCARB2 Gene Epilepsy, progressive myoclonic type 4, with or without renal failure NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with SCARB2 Gene Epilepsy, progressive myoclonic type 4, with or without renal failure
Test Details

The SCARB2 gene is associated with a rare genetic disorder called epilepsy, progressive myoclonic type 4, with or without renal failure. This disorder is characterized by seizures, muscle twitches or jerks (myoclonus), and progressive neurological decline. In some cases, it may also lead to kidney failure.

NGS genetic testing for this disorder involves sequencing the SCARB2 gene to identify any genetic mutations that may be causing the condition. This test can help diagnose the disorder and provide information about the severity of the condition and the risk of kidney failure. It can also help identify carriers of the genetic mutation, which can be useful for family planning. Treatment for this disorder typically involves managing symptoms with anticonvulsant medications and supportive care.