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SCN8A Gene Early infantile epileptic encephalopathy type 13 Genetic Test

4,400 د.إ

-21%

The SCN8A gene early infantile epileptic encephalopathy type 13 genetic test is a specialized diagnostic tool aimed at identifying mutations in the SCN8A gene, which have been linked to a severe form of epilepsy known as early infantile epileptic encephalopathy type 13 (EIEE13). This condition is characterized by frequent seizures that begin in the first months of life, often accompanied by developmental delays and other neurological issues. The SCN8A gene plays a crucial role in the functioning of brain cells, and mutations in this gene can disrupt the normal electrical activity in the brain, leading to epilepsy.

The test is available at DNA Labs UAE, a leading provider of genetic testing services in the United Arab Emirates. The cost of the test is 4400 AED, which reflects the specialized nature of the analysis and the sophisticated technology employed to accurately detect mutations in the SCN8A gene. By identifying these genetic mutations, the test can provide crucial information for the diagnosis and management of early infantile epileptic encephalopathy type 13, enabling healthcare providers to tailor treatment plans to the specific needs of their patients. This can include targeted therapies that may be more effective based on the patient’s genetic makeup, thereby improving outcomes and enhancing the quality of life for those affected by this challenging condition.

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SCN8A Gene Early Infantile Epileptic Encephalopathy Type 13 Genetic Test

Components: SCN8A Gene Early Infantile Epileptic Encephalopathy Type 13 Genetic Test

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 SCN8A Gene Early Infantile Epileptic Encephalopathy Type 13 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SCN8A Gene Early Infantile Epileptic Encephalopathy Type 13.

Test Details: The SCN8A gene is associated with early infantile epileptic encephalopathy type 13 (EIEE13), a rare genetic disorder characterized by seizures that begin in the first few months of life. NGS (next-generation sequencing) genetic testing can be used to analyze the SCN8A gene and detect any mutations or variants that may be causing EIEE13. This type of testing can help with early diagnosis, personalized treatment, and genetic counseling for affected individuals and their families.

Test Name SCN8A Gene Early infantile epileptic encephalopathy type 13 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 SCN8A Gene Early infantile epileptic encephalopathy type 13 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with SCN8A Gene Early infantile epileptic encephalopathy type 13
Test Details

The SCN8A gene is associated with early infantile epileptic encephalopathy type 13 (EIEE13), a rare genetic disorder characterized by seizures that begin in the first few months of life. NGS (next-generation sequencing) genetic testing can be used to analyze the SCN8A gene and detect any mutations or variants that may be causing EIEE13. This type of testing can help with early diagnosis, personalized treatment, and genetic counseling for affected individuals and their families.