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SIK1 Gene Early infantile epileptic encephalopathy type 30 Genetic Test

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The SIK1 gene plays a crucial role in the development and function of the nervous system. Mutations in this gene have been associated with Early Infantile Epileptic Encephalopathy Type 30 (EIEE30), a severe form of epilepsy that emerges in the first few months of life. This condition is characterized by frequent seizures and significant developmental delays, presenting a profound challenge for affected individuals and their families.

DNA Labs UAE offers a specialized genetic test to identify mutations in the SIK1 gene, providing crucial information for the diagnosis of EIEE30. The test is an important tool for clinicians in confirming the diagnosis, which can then guide treatment strategies and genetic counseling. Understanding the genetic basis of the condition can also help in predicting the course of the disease and in some cases, may inform treatment options.

The cost of the SIK1 gene test for Early Infantile Epileptic Encephalopathy Type 30 at DNA Labs UAE is 4400 AED. This investment covers the comprehensive analysis required to detect mutations in the SIK1 gene, providing families and healthcare providers with essential information for managing the condition. Given the complexity of EIEE30 and the significant impact it has on affected individuals, this genetic test represents a critical step in the journey towards better care and outcomes.

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SIK1 Gene Early Infantile Epileptic Encephalopathy Type 30 Genetic Test

Test Name: SIK1 Gene Early Infantile Epileptic Encephalopathy Type 30 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 SIK1 Gene Early Infantile Epileptic Encephalopathy Type 30 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SIK1 Gene Early Infantile Epileptic Encephalopathy Type 30.

Test Details

The SIK1 gene is associated with early infantile epileptic encephalopathy type 30, a rare genetic disorder that affects the brain and causes seizures in infants. NGS genetic testing can be used to analyze the SIK1 gene and identify mutations or variations that may be responsible for the disorder. This information can be used to diagnose the condition, provide genetic counseling to families, and inform treatment decisions.

NGS testing involves sequencing the entire gene and comparing it to a reference sequence to identify any variations or mutations. This type of testing is highly accurate and can provide valuable information for patients and healthcare providers.

Test Name SIK1 Gene Early infantile epileptic encephalopathy type 30 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 SIK1 Gene Early infantile epileptic encephalopathy type 30 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with SIK1 Gene Early infantile epileptic encephalopathy type 30
Test Details

The SIK1 gene is associated with early infantile epileptic encephalopathy type 30, a rare genetic disorder that affects the brain and causes seizures in infants. NGS genetic testing can be used to analyze the SIK1 gene and identify mutations or variations that may be responsible for the disorder. This information can be used to diagnose the condition, provide genetic counseling to families, and inform treatment decisions. NGS testing involves sequencing the entire gene and comparing it to a reference sequence to identify any variations or mutations. This type of testing is highly accurate and can provide valuable information for patients and healthcare providers.