The SLC17A5 gene is crucial for the proper functioning of the human body, particularly in the development and maintenance of healthy cells. Mutations in this gene can lead to a rare condition known as Sialuria Finnish type, which can have significant health implications for affected individuals. DNA Labs UAE offers a comprehensive genetic test for […]
In the realm of genetic testing, advancements have brought to light numerous conditions that were once shrouded in mystery. Among these, SESAME Syndrome stands out due to its rarity and the complexity of its symptoms. This condition, which is linked to mutations in the KCNJ10 gene, presents a unique set of challenges to both patients […]
In the realm of genetic testing and diagnosis, the advancements in understanding and identifying specific gene mutations have opened new pathways for managing and treating various conditions. One such area of significant development is in the field of neurology, specifically concerning seizures that occur in the neonatal period. A particular gene of interest in this […]
Understanding the nuances of genetic conditions is crucial for early diagnosis and effective management. One such condition that has garnered attention in the neonatal domain is seizures caused by mutations in the KCNQ2 gene, also known as Benign Neonatal Seizures Type 1. DNA Labs UAE, a leading genetic laboratory, offers a comprehensive genetic test specifically […]
Understanding the Symptoms of PRRT2 Gene Seizures Benign Familial Infantile Type 2 and the Importance of Genetic Testing Introduction to PRRT2 Gene Seizures Seizures in infants can be a terrifying experience for any parent, often leading to a desperate search for answers and solutions. Among the various types of seizures, those associated with the PRRT2 […]
Symptoms of TH Gene Segawa Syndrome Autosomal Recessive Genetic Test Segawa Syndrome, also known as Dopa-responsive dystonia (DRD), is a rare disorder that affects movement. It is characterized by a peculiar form of dystonia that typically begins in childhood. This disorder is linked to mutations in the Tyrosine Hydroxylase (TH) gene, which plays a critical […]
Schwartz-Jampel Syndrome (SJS) Type 1 is a rare genetic disorder characterized by muscle stiffness and abnormalities in bone development. It is caused by mutations in the HSPG2 gene, which plays a crucial role in the structural integrity and signaling functions of tissues. DNA Labs UAE offers a comprehensive genetic test for diagnosing this condition, ensuring […]
Symptoms of NOTCH4 Gene Schizophrenia Schizophrenia is a complex, chronic mental health disorder characterized by a range of symptoms that can affect a person’s thinking, feeling, and behavior. It is believed to be caused by a combination of genetic, brain chemistry, and environmental factors. Among the genetic contributors, the NOTCH4 gene has been identified as […]
Understanding the genetic underpinnings of psychiatric disorders is a rapidly evolving area within the field of medical research. Among the various genetic factors associated with the development of schizophrenia, the GRID2 gene has emerged as a significant point of interest. Schizophrenia is a complex mental disorder characterized by a range of symptoms, including delusions, hallucinations, […]
Schizophrenia is a complex mental disorder that affects how a person thinks, feels, and behaves. It is characterized by episodes of psychosis, including hallucinations and delusions, as well as cognitive impairments. The causes of schizophrenia are multifaceted, involving a combination of genetic, environmental, and neurological factors. Recent advancements in genetic research have shed light on […]
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.
