In the realm of genetic testing and diagnostics, the identification of specific gene mutations responsible for various conditions has revolutionized our approach to understanding and managing developmental delays and disorders. Among these, the GNAQ gene has been identified as a significant marker for certain developmental delays. At DNA Labs UAE, we offer a comprehensive GNAQ […]

In the realm of genetic research and testing, advancements have paved the way for early detection and intervention strategies for various genetic disorders. One such condition that has garnered attention is developmental delay and microcephaly, associated with mutations in the SLC1A4 gene. DNA Labs UAE stands at the forefront of this research, offering comprehensive genetic […]

Dentatorubral-pallidoluysian atrophy (DRPLA) is a rare, progressive genetic disorder that affects the brain. It is inherited in an autosomal dominant manner, meaning only one copy of the altered gene is necessary to cause the disorder. The ATN1 gene, located on chromosome 12, is responsible for DRPLA. Mutations in this gene lead to the production of […]

— Understanding the symptoms of OCRL Gene Dent Disease Type 2 and the significance of genetic testing is crucial for early diagnosis and management of the condition. Dent Disease, a rare genetic disorder, primarily affects the kidneys but can have systemic implications. The OCRL gene plays a vital role in this condition, and mutations in […]

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 […]

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 […]

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 […]

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 […]

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 […]

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 […]