Hyperekplexia, also known as “startle disease,” is a rare, inherited neurological disorder characterized by an exaggerated startle response. This condition can be due to mutations in several genes, one of which is the GLRB gene. The GLRB gene provides instructions for making a component of glycine receptors in the brain. These receptors are critical for […]
Symptoms of INPP5E Gene Joubert Syndrome Type 1 Joubert Syndrome is a rare genetic disorder that affects the development of the cerebellum, a part of the brain that regulates motor skills, balance, and coordination. Among the various genetic mutations that can cause Joubert Syndrome, mutations in the INPP5E gene lead to a specific subtype known […]
In the realm of genetic testing and diagnosis, understanding the intricacies of specific genes and their associated conditions is pivotal for both medical professionals and patients. One such gene that has garnered attention in recent years is the RETREG1 gene, which is linked to a rare condition known as Hereditary Sensory and Autonomic Neuropathy Type […]
Understanding ELP1 Gene HSAN3 Genetic Test Hereditary Sensory and Autonomic Neuropathy Type III (HSAN3), also known as Familial Dysautonomia, is a rare genetic disorder primarily affecting the development and function of the sensory and autonomic nervous systems. This condition, deeply impacting the lives of those diagnosed and their families, is traced back to mutations in […]
In the realm of medical genetics, the understanding and identification of genetic disorders have seen significant advancements. One such area of focus is the study of hereditary sensory and autonomic neuropathy type IV (HSAN IV), also known as congenital insensitivity to pain with anhidrosis (CIPA). This condition is primarily caused by mutations in the NTRK1 […]
In the realm of genetic testing, advancements have paved the way for identifying and understanding a myriad of genetic conditions that were once shrouded in mystery. Among these, the NGF Gene HSAN5 Genetic Test stands out as a pivotal development, offering insights into a rare but significant genetic disorder. This test, available at DNA Labs […]
Understanding the symptoms associated with PRDM12 Gene HSAN8 is crucial for individuals who may be at risk of this rare but significant genetic condition. Hereditary Sensory and Autonomic Neuropathy Type VIII (HSAN8) is a disorder affecting the nervous system, leading to a range of sensory deficits and autonomic dysfunction. The PRDM12 gene, when mutated, is […]
Understanding the Symptoms of KIF1A Gene HSN2C The KIF1A gene is critical in the human body for its role in transporting synaptic vesicles in nerve cells. Mutations in this gene can lead to a rare neurological disorder known as Hereditary Sensory and Autonomic Neuropathy Type 2C (HSN2C). This condition affects the peripheral nervous system, which […]
Symptoms of HTT Gene Huntington Disease Genetic Test Huntington’s disease (HD) is a progressive brain disorder caused by a defective gene. This disease affects muscle coordination and leads to mental decline and behavioral symptoms. Symptoms of the disease can vary widely among affected individuals, even within the same family. The HTT gene Huntington disease genetic […]
— Huntington’s disease is a progressive brain disorder caused by a defective gene. This disease affects the brain, causing gradual physical, cognitive, and psychological deterioration. A particular gene known as ZDHHC17 has been closely associated with this condition. Understanding the symptoms of Huntington’s disease related to the ZDHHC17 gene is crucial for early diagnosis and […]
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.
