Understanding GSS Gene Glutathione Synthetase Deficiency Glutathione synthetase deficiency, caused by mutations in the GSS gene, is a rare genetic disorder that affects the body’s ability to produce glutathione. Glutathione is a critical antioxidant that plays a key role in protecting cells from oxidative damage and maintaining the immune system. Individuals with this deficiency can […]
The GSTT1 gene is responsible for encoding an enzyme known as Glutathione S-transferase theta-1 (GSTT1), which plays a crucial role in the detoxification process within the human body. This enzyme helps in metabolizing xenobiotics, which are foreign chemical substances not naturally produced by the body, and various carcinogens. A deficiency in the GSTT1 gene can […]
Genetic testing has become a cornerstone in the diagnosis and management of various inherited disorders. One such condition that has garnered attention is Glutaric aciduria type 3, linked to mutations in the SUGCT gene. DNA Labs UAE is at the forefront of providing comprehensive genetic testing services, including for Glutaric aciduria type 3. This article […]
Genetic testing has become an essential part of modern healthcare, offering insights into inherited conditions and enabling early intervention. Among the various genetic disorders, Glutaric Acidemia Type 2C, caused by mutations in the ETFDH gene, is a condition that can have significant health implications. DNA Labs UAE is at the forefront of providing comprehensive genetic […]
Symptoms of GCDH Gene Glutaric Acidemia Type 1 Glutaric acidemia type 1 is a rare genetic disorder that affects the body’s ability to process certain types of amino acids properly. This condition is caused by mutations in the GCDH gene, leading to an accumulation of harmful substances in the body, which can damage the brain […]
In the realm of genetic testing, the understanding and identification of specific gene deficiencies have become crucial in diagnosing and treating various congenital conditions. One such condition, caused by deficiencies in the GLUL gene, can lead to severe health implications if not identified and managed properly. The GLUL gene is responsible for the synthesis of […]
Symptoms of FTCD Gene Glutamate Formiminotransferase Deficiency Glutamate formiminotransferase deficiency is a rare genetic disorder caused by mutations in the FTCD gene. This condition affects the body’s ability to process certain amino acids, leading to a range of symptoms that can impact an individual’s health and quality of life. Understanding these symptoms is crucial for […]
Symptoms of SLC5A1 Gene Glucose-Galactose Malabsorption Genetic Test Glucose-Galactose Malabsorption (GGM) is a rare genetic disorder that impacts the body’s ability to absorb glucose and galactose, two primary sugars found in our diet. This condition is caused by mutations in the SLC5A1 gene, which plays a crucial role in the absorption of glucose and galactose […]
In the realm of genetic diagnostics, the ability to pinpoint specific genetic disorders has transformed the landscape of medical science and patient care. Among these advancements, the identification of mutations within the NNT gene, which can lead to glucocorticoid deficiency type 4 with or without mineralocorticoid deficiency, represents a critical step forward. DNA Labs UAE […]
In the realm of genetic testing and diagnostics, the MRAP gene glucocorticoid deficiency type 2 stands out as a significant concern for many individuals and families. This condition, rooted in genetic anomalies, manifests through a spectrum of symptoms that necessitate a comprehensive understanding and approach for management and treatment. DNA Labs UAE, a leading entity […]
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.
