Symptoms and Testing information for SCN2A Gene Convulsions Benign Familial Infantile 3 Genetic Test

Symptoms and Testing information for SCN2A Gene Convulsions Benign Familial Infantile 3 Genetic Test

The SCN2A gene is critical in the development and function of the nervous system, playing a pivotal role in the regulation of electrical signals in the brain. Mutations in this gene are linked to a range of neurological conditions, including Convulsions Benign Familial Infantile 3 (BFIC3). This condition, while rare, is significant for the families it affects, presenting in the early months of life and often causing considerable concern. Understanding the symptoms, implications, and available genetic testing options, such as those offered by DNA Labs UAE, is essential for affected families.

Symptoms of SCN2A Gene Convulsions Benign Familial Infantile 3

The symptoms associated with SCN2A Gene Convulsions Benign Familial Infantile 3 are varied but generally revolve around the central nervous system’s function. Key symptoms include:

  • Early Onset: Symptoms typically manifest within the first six months of life, often presenting as a sudden onset of seizures.
  • Seizure Characteristics: The seizures associated with BFIC3 are usually brief but can be frequent. They often occur in clusters, with multiple episodes happening in a short period.
  • Developmental Impact: While most children with BFIC3 do not experience developmental delays, some affected individuals may face challenges in their cognitive or physical development.
  • Family History: BFIC3 is inherited in an autosomal dominant pattern, meaning a family history of similar symptoms could be a significant indicator.

Recognizing these symptoms early can be crucial in managing the condition effectively and mitigating any potential developmental impacts.

Genetic Testing for SCN2A Gene Convulsions Benign Familial Infantile 3

Genetic testing has emerged as a vital tool in diagnosing and understanding BFIC3. DNA Labs UAE offers a comprehensive SCN2A Gene Convulsions Benign Familial Infantile 3 Genetic Test, designed to identify mutations in the SCN2A gene that could lead to this condition. This test is not only instrumental in confirming a diagnosis but also in informing treatment strategies and understanding the risk of recurrence in future offspring.

The test cost at DNA Labs UAE is set at 4400 AED, reflecting the intricate processes involved in genetic analysis and the invaluable insights it provides to affected families. It is a small price to pay for the peace of mind and clarity that comes with understanding one’s genetic makeup and its implications on health.

Why Choose DNA Labs UAE?

Choosing where to undergo genetic testing is a significant decision. DNA Labs UAE stands out for several reasons:

  • Expertise: With a team of highly qualified professionals, DNA Labs UAE ensures accurate and reliable testing outcomes.
  • Comprehensive Testing: Beyond the SCN2A Gene Convulsions Benign Familial Infantile 3 Genetic Test, DNA Labs UAE offers a wide range of genetic tests, catering to various conditions and needs.
  • Support and Counseling: Understanding genetic test results can be challenging. DNA Labs UAE provides expert counseling to help individuals and families interpret their results and understand their implications.
  • Confidentiality: DNA Labs UAE upholds the highest standards of privacy and confidentiality, ensuring that personal information and test results are securely managed.

In conclusion, the SCN2A Gene Convulsions Benign Familial Infantile 3 Genetic Test offered by DNA Labs UAE is a critical resource for families affected by this condition. By identifying the presence of specific gene mutations, families can gain invaluable insights into their health, informing their decisions and allowing for a better understanding of their condition. With a cost of 4400 AED, this test is an investment in health and peace of mind, backed by the expertise and support of DNA Labs UAE.

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