Symptoms and Testing information for CHRNB2 Gene Epilepsy nocturnal frontal lobe type 3 Genetic Test

Symptoms and Testing information for CHRNB2 Gene Epilepsy nocturnal frontal lobe type 3 Genetic Test

Epilepsy is a neurological condition characterized by recurrent seizures, which are sudden surges of electrical activity in the brain. Among its various types, Nocturnal Frontal Lobe Epilepsy (NFLE) presents a unique pattern, primarily occurring during sleep. Type 3 NFLE, associated with mutations in the CHRNB2 gene, is a rare but significant form, necessitating precise diagnostic approaches to tailor effective treatment strategies. DNA Labs UAE stands at the forefront of genetic testing, offering a comprehensive CHRNB2 Gene Epilepsy Nocturnal Frontal Lobe Type 3 Genetic Test, priced at 4400 AED, to aid in the accurate diagnosis of this condition.

Symptoms of CHRNB2 Gene Epilepsy Nocturnal Frontal Lobe Type 3

The clinical manifestations of CHRNB2-related NFLE can be diverse, with symptoms primarily occurring during sleep, which may sometimes extend into the waking hours. Recognizing these symptoms is crucial for early diagnosis and management.

  • Complex Motor Behaviors: Individuals may exhibit complex, often bizarre, motor behaviors during sleep, which are typically semi-purposeful and may include ambulation, dystonic posturing, or even violent movements.
  • Paroxysmal Arousals: Sudden, brief awakenings from sleep with confusion and disorientation are common. These episodes can be frequent and may significantly disrupt sleep quality.
  • Autonomic Manifestations: Symptoms such as heart palpitations, sweating, and flushing may accompany seizures, indicating autonomic nervous system involvement.
  • Nocturnal Seizures: Seizures primarily occur during sleep, often in the early phases of the night. They may, however, also manifest during daytime naps or, less frequently, during wakefulness.
  • Postictal Symptoms: Following a seizure, individuals may experience tiredness, headache, or confusion, which can last for several hours.
  • Family History: A family history of epilepsy, particularly NFLE, may be present, suggesting a genetic predisposition.

Importance of Genetic Testing for CHRNB2 Gene Epilepsy

Genetic testing plays a pivotal role in the diagnosis and management of CHRNB2 Gene Epilepsy Nocturnal Frontal Lobe Type 3. By identifying the specific genetic mutation, clinicians can tailor treatment strategies to the individual’s genetic profile, potentially improving outcomes. Furthermore, genetic testing can aid in the differential diagnosis, distinguishing CHRNB2-related epilepsy from other sleep disorders or types of epilepsy, thereby avoiding unnecessary treatments and focusing on the most effective interventions.

The CHRNB2 Gene Epilepsy Nocturnal Frontal Lobe Type 3 Genetic Test at DNA Labs UAE

DNA Labs UAE offers a specialized genetic test for CHRNB2 Gene Epilepsy Nocturnal Frontal Lobe Type 3, priced at 4400 AED. This test is a critical tool for clinicians in the diagnosis and management of this specific type of epilepsy. Utilizing advanced genetic sequencing technologies, the test accurately identifies mutations in the CHRNB2 gene, providing a solid foundation for personalized treatment plans.

Early diagnosis and intervention are key to managing CHRNB2-related epilepsy effectively. With the comprehensive genetic testing services provided by DNA Labs UAE, patients and their families can gain invaluable insights into their condition, enabling them to make informed decisions about their health and treatment options.


Epilepsy, particularly the nocturnal frontal lobe type associated with the CHRNB2 gene, presents unique challenges in diagnosis and management. The availability of genetic testing, such as the CHRNB2 Gene Epilepsy Nocturnal Frontal Lobe Type 3 Genetic Test offered by DNA Labs UAE, represents a significant advancement in the field. By identifying the genetic underpinnings of this condition, healthcare providers can offer targeted treatments, improving the quality of life for those affected. Priced at 4400 AED, this test is a valuable investment in the pursuit of personalized medicine, ensuring that patients receive the most effective care tailored to their genetic makeup.

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