Symptoms and Testing information for EEF1A2 Gene Early infantile epileptic encephalopathy type 33 Genetic Test

Symptoms and Testing information for EEF1A2 Gene Early infantile epileptic encephalopathy type 33 Genetic Test

Understanding the symptoms and implications of early infantile epileptic encephalopathy type 33 (EIEE33) is crucial for families and healthcare providers. This rare but severe condition, associated with mutations in the EEF1A2 gene, can lead to significant developmental challenges and neurological issues in affected infants. DNA Labs UAE offers a comprehensive genetic test for EIEE33, providing essential information for diagnosis and management. This article delves into the symptoms of EIEE33, the importance of the EEF1A2 gene, and details regarding the genetic test available at DNA Labs UAE, including its cost.

Symptoms of Early Infantile Epileptic Encephalopathy Type 33 (EIEE33)

EIEE33 is characterized by a range of neurological symptoms that manifest early in infancy. These symptoms are often severe and can significantly impact the quality of life of affected individuals and their families. Key symptoms include:

  • Severe developmental delay: Children with EIEE33 typically exhibit profound delays in reaching developmental milestones. This can include delays in motor skills, speech, and social abilities.
  • Epileptic seizures: Recurrent seizures are a hallmark of EIEE33. These seizures are often resistant to standard epilepsy treatments, making management challenging.
  • Spasticity: Muscle stiffness and spasms are common in individuals with EIEE33, contributing to the difficulty in movement and coordination.
  • Intellectual disability: Most affected individuals will experience some degree of intellectual disability, which can range from mild to severe.

Early diagnosis and intervention are critical in managing the symptoms of EIEE33 and improving the quality of life for affected individuals.

Importance of the EEF1A2 Gene

The EEF1A2 gene plays a significant role in protein synthesis within cells, particularly in the brain and nervous system. Mutations in this gene disrupt normal protein synthesis, leading to the neurological symptoms observed in EIEE33. Understanding the genetic basis of EIEE33 is crucial for accurate diagnosis, potential treatment options, and genetic counseling for families.

EEF1A2 Gene Early Infantile Epileptic Encephalopathy Type 33 Genetic Test at DNA Labs UAE

DNA Labs UAE offers a comprehensive genetic test for EIEE33, targeting mutations in the EEF1A2 gene. This test is vital for confirming the diagnosis of EIEE33, especially in infants presenting with the characteristic symptoms of the condition. The genetic test involves a simple blood sample from the affected individual and utilizes advanced sequencing technologies to identify mutations in the EEF1A2 gene.

The cost of the EEF1A2 gene early infantile epileptic encephalopathy type 33 genetic test at DNA Labs UAE is 4400 AED. While the cost may seem significant, the value of an accurate diagnosis cannot be overstated. It provides a clear path for management and support, and in some cases, may guide treatment options.

Conclusion

Early infantile epileptic encephalopathy type 33 is a challenging condition, but understanding its symptoms and genetic basis can significantly improve the management and support for affected individuals and their families. The EEF1A2 gene test offered by DNA Labs UAE is a crucial step towards a definitive diagnosis, providing families with the information they need to navigate the complexities of this condition. For more information about the test and to schedule an appointment, visit DNA Labs UAE.

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