Symptoms of ITM2B Gene Dementia Familial British Type Genetic Test Dementia Familial British Type, also known as Familial British Dementia (FBD), is a rare genetic disorder caused by mutations in the ITM2B gene. This condition is inherited in an autosomal dominant pattern, meaning that only one copy of the altered gene in each cell is […]
Understanding the complexities of genetic disorders is crucial for early diagnosis and management. Among these, Dravet Syndrome stands out due to its severe implications on those affected. This condition, primarily caused by mutations in the SCN2A gene, leads to a spectrum of symptoms that can significantly impact the quality of life. At DNA Labs UAE, […]
Dementia is a broad category of brain diseases that cause a long-term and often gradual decrease in the ability to think and remember. Familial Danish Dementia (FDD), a very rare form of dementia, is caused by mutations in the ITM2B gene. Recognizing the symptoms of this condition is crucial for early diagnosis and management. At […]
Dravet Syndrome is a severe form of epilepsy that begins in infancy. It is characterized by frequent, prolonged seizures often triggered by high temperatures or fever. However, the discovery of the role of the SCN9A gene as a modifier in Dravet Syndrome has opened new avenues for understanding and managing this condition. At DNA Labs […]
Dementia, a term that encompasses a range of cognitive decline conditions, can be a daunting diagnosis for patients and their families. Among its various forms, Frontotemporal Dementia (FTD) is particularly challenging due to its early onset and rapid progression. Understanding the genetic underpinnings of this condition, such as mutations in the GRN gene, can provide […]
Symptoms of FRRS1L Gene Dysautonomia Dysautonomia associated with the FRRS1L gene presents a complex and multifaceted condition that affects the autonomic nervous system, which controls the involuntary functions of the body, including heart rate, blood pressure, and digestion. This condition can lead to a wide range of symptoms, significantly impacting the quality of life of […]
Frontotemporal dementia (FTD) is a group of disorders caused by progressive nerve cell loss in the brain’s frontal lobes (the areas behind your forehead) or its temporal lobes (the regions behind your ears). The MAPT gene, which provides instructions for making a protein called tau, plays a crucial role in the development of some forms […]
Understanding the genetic underpinnings of dementia, particularly frontotemporal dementia (FTD), is crucial for early diagnosis and management. One gene that has been closely associated with an increased risk of developing FTD is the PSEN1 gene. Mutations in this gene can lead to the early onset of dementia, which is why genetic testing for the PSEN1 […]
Symptoms of TARDBP Gene Dementia Frontotemporal Genetic Test Frontotemporal Dementia (FTD) is a form of dementia that is distinct from other types, such as Alzheimer’s disease, in its symptoms, causes, and patterns of brain degeneration. One of the genetic markers linked to an increased risk of developing FTD is mutations in the TARDBP gene. Understanding […]
Dementia with Lewy bodies (DLB) is a type of progressive dementia that leads to a decline in thinking, reasoning, and independent function because of abnormal microscopic deposits that damage brain cells over time. Among the genetic factors associated with DLB, variations in the SNCA gene have garnered significant attention. The SNCA gene provides instructions for […]
DNA Labs UAE is a leading provider of genomics services in the United Arab Emirates. Our comprehensive range of services includes DNA sequencing, gene expression analysis, and SNP genotyping. With state-of-the-art equipment and a dedicated team of scientists and technicians, we ensure high-quality, accurate, and reliable data.
