Epilepsy is a neurological condition characterized by recurrent seizures, which are sudden bursts of electrical activity in the brain affecting how it works for a short period. Among the various types of epilepsy, Nocturnal Frontal Lobe Epilepsy (NFLE) stands out due to its unique manifestation primarily during sleep. A significant breakthrough in understanding the genetic […]

Epilepsy is a neurological disorder marked by recurrent, unprovoked seizures. Among its various forms, nocturnal frontal lobe epilepsy (NFLE) presents a unique challenge due to its manifestation primarily during sleep. Recent advancements in genetics have identified the KCNT1 gene as a significant contributor to certain epilepsy syndromes, including NFLE. Understanding the symptoms of KCNT1 gene […]

Epilepsy is a neurological disorder characterized by recurrent seizures. Among the various types of epilepsy, Juvenile Absence Epilepsy (JAE) is a condition that typically begins in childhood or adolescence. It is crucial to understand the genetic underpinnings of such disorders to provide accurate diagnoses and personalized treatment plans. In this context, the EFHC1 gene plays […]

Epilepsy is a neurological disorder marked by an enduring predisposition to generate epileptic seizures. It’s a condition that affects millions worldwide, with various underlying genetic factors contributing to its complexity. Among the genetic factors, mutations in the SLC2A1 gene have been identified as a significant cause of epilepsy, specifically idiopathic generalized epilepsy type 12. Recognizing […]

Understanding the symptoms of CLCN2 gene epilepsy, specifically idiopathic generalized type 11, is crucial for individuals and families who may be at risk. This genetic condition is linked to a mutation in the CLCN2 gene, which plays a significant role in the functioning of chloride channels in the body. These channels are essential for the […]

Epilepsy is a neurological disorder characterized by recurrent, unprovoked seizures. Idiopathic generalized epilepsy (IGE) represents a group of epileptic disorders that are believed to have a strong genetic component. Among the genes linked to IGE, the GABRD gene has been identified as a significant contributor to the condition known as Epilepsy, Idiopathic Generalized, Type 10. […]

Epilepsy, hearing loss, and mental retardation syndrome, linked to mutations in the SPATA5 gene, presents a complex set of challenges for affected individuals and their families. Understanding the symptoms and genetic underpinnings of this condition is crucial for timely diagnosis and management. DNA Labs UAE offers a comprehensive genetic testing service to help identify mutations […]

Epilepsy is a neurological disorder marked by an enduring predisposition to generate epileptic seizures and by the neurobiological, cognitive, psychological, and social consequences of this condition. The complexity of epilepsy is further amplified by the existence of various genetic components that can influence its manifestation. Among these genetic factors, the HCN2 gene has been identified […]

Epilepsy is a neurological condition that affects millions of people around the world, characterized by recurrent seizures. Among the various genetic factors contributing to the development of epilepsy, mutations in the SCN3A gene have been identified as a significant cause of focal epilepsy. Focal seizures, also known as partial seizures, originate in just one part […]

Epilepsy is a neurological disorder marked by an enduring predisposition to generate epileptic seizures. It’s a condition that can affect anyone, regardless of age, race, or background. Familial Temporal Lobe Epilepsy Type 7 (FTLE7) represents a specific subtype of epilepsy, distinguished by its genetic origins and particular symptomatic manifestations. One of the genes implicated in […]