In the realm of genetic diagnostics and personalized medicine, understanding the nuances of specific genetic conditions is paramount. One such condition, Fabry disease, caused by mutations in the GLA gene, has garnered significant attention due to its wide range of symptoms and the critical importance of early detection. DNA Labs UAE stands at the forefront […]
Genetic testing has become a cornerstone in the diagnosis and management of various inherited disorders. Among these, the SLC16A1 gene erythrocyte lactate transporter defect is a condition that has garnered attention due to its impact on lactate transport in red blood cells. This article provides an in-depth look at the symptoms associated with this genetic […]
Symptoms of TMPRSS15 Gene Enterokinase Deficiency Genetic Test The TMPRSS15 gene plays a crucial role in the human body, encoding for the enzyme enterokinase, which is essential for the digestion of proteins. A deficiency in this gene can lead to a range of symptoms and health issues, necessitating accurate diagnosis and management. DNA Labs UAE […]
Symptoms of CYP2B6 Gene Efavirenz Poor Metabolism of Genetic Test The CYP2B6 gene plays a pivotal role in the metabolism of various substances within the body, including the antiretroviral medication, Efavirenz, which is commonly used in the treatment of HIV. Variations in the CYP2B6 gene can lead to poor metabolism of Efavirenz, resulting in higher […]
Symptoms of DYM Gene Dyggve-Melchior-Clausen Disease Dyggve-Melchior-Clausen (DMC) disease is a rare genetic disorder that affects bone development and structure, leading to skeletal dysplasia. This condition is caused by mutations in the DYM gene, which plays a crucial role in the development and maintenance of healthy bone and cartilage. Individuals with DMC disease exhibit a […]
Symptoms of DMGDH Gene Dimethylglycine Dehydrogenase Deficiency Dimethylglycine Dehydrogenase (DMGDH) deficiency is a rare genetic disorder that affects the body’s ability to metabolize certain amino acids properly. This condition can lead to a variety of health issues, ranging from mild to severe. Recognizing the symptoms early can be crucial for managing the condition effectively. Some […]
Dihydropyrimidinuria is a rare genetic disorder that affects the body’s ability to break down certain components of proteins, specifically the pyrimidine bases of uracil and thymine. This condition is caused by mutations in the DPYS gene, which is crucial for the normal function of the enzyme dihydropyrimidine dehydrogenase (DPD). DPD plays a vital role in […]
In the realm of personalized medicine, genetic testing plays a pivotal role in understanding an individual’s susceptibility to various conditions and their response to certain medications. One such critical genetic test is for DPYD gene dihydropyrimidine dehydrogenase deficiency. This deficiency can significantly impact the body’s ability to metabolize certain chemotherapy drugs, leading to severe and […]
The NEUROG3 gene plays a pivotal role in the development of the endocrine pancreas and is crucial for the differentiation of enteroendocrine cells in the gastrointestinal tract. Mutations in the NEUROG3 gene can lead to a rare but severe disorder known as congenital malabsorptive diarrhea type 4. This condition is characterized by a range of […]
Diarrhea type 3 secretory sodium congenital syndromic, often referred to as congenital sodium diarrhea (CSD), is a rare genetic disorder that affects the body’s ability to properly absorb sodium through the intestines. This condition is caused by mutations in the SPINT2 gene, which plays a crucial role in the regulation of sodium channels in the […]
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.
