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 […]
Neurology Diseases
Symptoms and Testing information for GRIN2A Gene Epilepsy with neurodevelopmental defects Genetic Test
Epilepsy is a neurological condition that affects millions of people worldwide, manifesting in recurrent, unprovoked seizures. Among the various forms of epilepsy, genetic factors play a significant role in its development and progression. One such genetic factor is mutations in the GRIN2A gene, which have been associated with epilepsy accompanied by neurodevelopmental defects. Understanding the […]
Symptoms and Testing information for KCNT1 Gene Epilepsy nocturnal frontal lobe Genetic Test
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 […]
Symptoms and Testing information for GABRG2 Gene Epilepsy childhood absence type 2 Genetic Test
Epilepsy is a neurological condition characterized by recurrent seizures. Among its various types, Childhood Absence Epilepsy (CAE) is notable for its impact on children, typically between the ages of 4 and 8 years. A significant development in understanding this condition has been the identification of genetic factors that contribute to its manifestation. One such gene, […]
Symptoms and Testing information for CHRNA4 Gene Epilepsy nocturnal frontal lobe type 1 Genetic Test
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 […]
Symptoms and Testing information for GABRA1 Gene Epilepsy childhood absence type 4 susceptibility to Genetic Test
Epilepsy is a neurological disorder marked by an enduring predisposition to generate epileptic seizures. It is a condition that affects millions of people worldwide, with various genetic factors playing a crucial role in its development. One such genetic factor is related to the GABRA1 gene, which has been linked to childhood absence epilepsy type 4 […]
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 […]
Symptoms and Testing information for GABRB3 Gene Epilepsy childhood absence type 5 Genetic Test
At DNA Labs UAE, we are dedicated to providing comprehensive genetic testing services that cater to a wide range of conditions, including epilepsy. One particular focus is on the GABRB3 gene, which has been linked to childhood absence epilepsy type 5. This condition, while specific, affects numerous families and understanding its symptoms can be crucial […]
Symptoms and Testing information for CACNA1H Gene Epilepsy childhood absence type 6 susceptibility to Genetic Test
In the realm of genetic testing and personalized medicine, understanding the intricacies of specific genes and their impact on our health has become increasingly important. One such gene that has garnered attention is the CACNA1H gene, which is linked to epilepsy childhood absence type 6 susceptibility. DNA Labs UAE is at the forefront of providing […]
Symptoms and Testing information for DEPDC5 Gene Epilepsy familial focal with variable foci Genetic Test
Epilepsy is a neurological disorder characterized by recurrent seizures, which are brief episodes of involuntary movement that may involve a part of the body (partial) or the entire body (generalized), and are sometimes accompanied by loss of consciousness and control of bowel or bladder function. Familial Focal Epilepsy with Variable Foci (FFEVF) is a particular […]