Epilepsy is a neurological condition characterized by recurrent, unprovoked seizures. Among its various types, familial temporal lobe epilepsy (FTLE) is particularly noteworthy due to its genetic basis. Temporal lobe epilepsy is one of the most common forms of epilepsy and can be further categorized based on its cause and characteristics. One of the genetic variations […]

Epilepsy is a neurological condition characterized by recurrent seizures, affecting millions of people worldwide. Familial Temporal Lobe Epilepsy type 1 (FTLE1) is a specific subtype of epilepsy that has a genetic basis. This condition is particularly associated with mutations in the LGI1 gene. Understanding the symptoms of LGI1 Gene Epilepsy and the significance of genetic […]

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 […]

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 […]

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 […]

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 […]

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, […]

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 […]

Epidermolysis Bullosa Simplex (EBS) is a group of genetic conditions that result in easy blistering of the skin and mucous membranes in response to minor injury or friction. Among the various types of EBS, the Autosomal Recessive Type 2, also known as the severe generalized type, is caused by mutations in the DST gene. This […]

Epidermolysis Bullosa Simplex with Muscular Dystrophy (EBS-MD) is a rare genetic disorder that affects the skin and muscles. It is caused by mutations in the PLEC gene, which plays a critical role in the integrity of skin cells and muscle tissue. Individuals with this condition often experience a wide range of symptoms, which can vary […]