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DNM1 Gene Early infantile epileptic encephalopathy type 31 Genetic Test

4,400 د.إ

-21%

The DNM1 Gene Early Infantile Epileptic Encephalopathy Type 31 Genetic Test is a specialized diagnostic examination offered by DNA Labs UAE, designed to detect mutations in the DNM1 gene, which have been associated with Early Infantile Epileptic Encephalopathy Type 31 (EIEE31). This condition is a severe form of epilepsy that manifests in infancy and is characterized by frequent seizures and significant developmental delays. The test plays a crucial role in the early identification of this genetic disorder, enabling healthcare providers to initiate appropriate treatment and management strategies as early as possible.

The testing process involves collecting a DNA sample from the patient, typically through a blood draw or a cheek swab, which is then analyzed in the laboratory for any genetic abnormalities in the DNM1 gene. Positive identification of mutations can help in confirming the diagnosis of EIEE31, facilitating a better understanding of the condition’s progression and the potential response to various treatment options.

The cost of the DNM1 Gene Early Infantile Epileptic Encephalopathy Type 31 Genetic Test at DNA Labs UAE is 4400 AED. This investment covers the comprehensive analysis required to detect the specific genetic mutation associated with this condition. By choosing DNA Labs UAE for this critical testing, patients and their families gain access to advanced genetic testing technology and expertise, ensuring accurate and reliable results that can significantly impact the management and outcome of the condition.

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  • This test is not intended for medical diagnosis or treatment
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DNM1 Gene Early Infantile Epileptic Encephalopathy Type 31 Genetic Test

At DNA Labs UAE, we offer the DNM1 Gene Early Infantile Epileptic Encephalopathy Type 31 Genetic Test for the diagnosis of a rare genetic disorder characterized by seizures that begin in the first few months of life. This test is designed to identify any mutations in the DNM1 gene, which is associated with early infantile epileptic encephalopathy type 31 (EIEE31).

Test Details

The DNM1 gene provides instructions for making a protein involved in the process of endocytosis, which is the uptake of materials into cells. Mutations in this gene can cause EIEE31. Our NGS genetic testing method involves sequencing the DNM1 gene to identify any mutations that may be causing the condition.

Test Components and Price

The DNM1 Gene Early Infantile Epileptic Encephalopathy Type 31 Genetic Test is priced at 4400.0 AED. The test requires a blood sample or extracted DNA, or one drop of blood on an FTA card.

Report Delivery and Test Type

After the sample is collected, the report will be delivered within 3 to 4 weeks. This test falls under the category of neurological disorders and is conducted by our specialized Genetics department.

Doctor and Pre Test Information

This test is recommended for patients with a clinical history of early infantile epileptic encephalopathy type 31. We advise patients to consult with a neurologist and undergo a genetic counseling session to draw a pedigree chart of family members affected by the condition.

Treatment and Supportive Care

If diagnosed with EIEE31, the typical treatment involves the use of antiepileptic medications and supportive care. Our test can not only aid in the diagnosis of the disorder but also provide information about the risk of passing it on to future children.

Test Name DNM1 Gene Early infantile epileptic encephalopathy type 31 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 DNM1 Gene Early infantile epileptic encephalopathy type 31 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with DNM1 Gene Early infantile epileptic encephalopathy type 31
Test Details

The DNM1 gene is associated with early infantile epileptic encephalopathy type 31 (EIEE31), a rare genetic disorder characterized by seizures that begin in the first few months of life. The condition is caused by mutations in the DNM1 gene, which provides instructions for making a protein involved in the process of endocytosis, the uptake of materials into cells.

NGS genetic testing for EIEE31 involves sequencing the DNM1 gene to identify any mutations that may be causing the condition. This test can be helpful in diagnosing the disorder, as well as providing information about the risk of passing the condition on to future children. Treatment for EIEE31 typically involves antiepileptic medications and supportive care.