Symptoms of SLC35C1 Gene Glycosylation Disorder Type 2C Genetic Test Glycosylation is a critical biological process where sugars are attached to proteins and lipids, altering their function and stability. One rare disorder associated with this process is the SLC35C1 gene glycosylation disorder, also known as Congenital Disorder of Glycosylation Type 2C (CDG2C). This condition results […]
Symptoms of MGAT2 Gene Glycosylation Disorder Type 2A Congenital disorders of glycosylation (CDG) are a group of rare genetic conditions that affect a complex process in the body called glycosylation, which is crucial for the proper function of many proteins and fats. The MGAT2 gene glycosylation disorder, also known as CDG Type IIa, is one […]
Glycine encephalopathy, also known as non-ketotic hyperglycinemia (NKH), is a rare genetic disorder that affects the body’s ability to break down the amino acid glycine. This condition is caused by mutations in several genes, including the GCSH gene. It leads to an accumulation of glycine in the body, which can cause severe neurological symptoms. DNA […]
DNA Labs UAE is at the forefront of genetic testing and diagnostics, offering a comprehensive range of services designed to provide individuals with crucial insights into their genetic makeup. Among these, the AMT Gene Glycine Encephalopathy Genetic Test stands out for its significance in diagnosing a rare but serious condition. This article delves into the […]
GLUT1 Deficiency Syndrome Type 1 is a rare genetic disorder that affects the body’s ability to transport glucose into the brain, leading to a range of neurological symptoms. The condition is caused by mutations in the SLC2A1 gene, which encodes the glucose transporter protein GLUT1. Early diagnosis and management are crucial for improving the quality […]
Gillespie Syndrome, a rare genetic disorder, is characterized by aniridia (partial or complete absence of the iris), cerebellar ataxia (lack of muscle coordination affecting speech, eye movements, and the ability to swallow), and intellectual disability. Recent studies have pinpointed mutations in the ITPR1 gene as a primary cause of this condition. DNA Labs UAE offers […]
Giant Axonal Neuropathy (GAN) Type 1 is a rare genetic disorder that affects the nervous system. The disorder is characterized by a progressive loss of nerve function, which typically begins in childhood. It is caused by mutations in the GAN gene, which plays a crucial role in maintaining the structure and function of nerve cells. […]
Gerstmann-Straussler-Scheinker disease (GSS) is a rare, inherited neurodegenerative disorder that is caused by mutations in the PRNP gene. This condition is classified under a group of diseases known as prion diseases, which affect the normal folding of prion proteins in the brain, leading to brain damage. The symptoms of GSS can vary widely among affected […]
At DNA Labs UAE, we are dedicated to providing comprehensive genetic testing services to help individuals and families understand their genetic health. One of the specialized tests we offer focuses on the STX1B gene, which has been linked to Generalized Epilepsy with Febrile Seizures Plus Type 9 (GEFS+ Type 9). This condition is a form […]
Understanding the nuances of genetic disorders is crucial for effective diagnosis and treatment. Among these, the SCN9A gene plays a significant role in the development of Generalized Epilepsy with Febrile Seizures Plus Type 7 (GEFS+7). This condition, marked by a spectrum of seizure types, often requires precise genetic testing for accurate identification. DNA Labs UAE […]
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.
