In the complex and ever-evolving field of genetics, understanding the intricate details of specific conditions can be a gateway to tailored healthcare and improved outcomes. Among these conditions, intraheptic cholestasis of pregnancy (ICP) stands out due to its potential impact on pregnant individuals and their unborn children. The ATP8B1 gene cholestasis intrahepatic of pregnancy type […]
Cholestasis is a condition characterized by the reduction or stoppage of bile flow from the liver to the duodenum. Among its various types, Benign Recurrent Intrahepatic Cholestasis (BRIC) associated with the ATP8B1 gene is a rare genetic disorder. This condition can lead to significant discomfort and health issues for those affected. DNA Labs UAE offers […]
The ABCB4 gene plays a crucial role in the body, particularly in the liver. It is responsible for producing a protein that helps move bile acids out of liver cells. When there is a mutation in this gene, it can lead to a condition known as progressive intrahepatic cholestasis type 3. This condition is characterized […]
Cholestasis is a liver condition that slows or stops the flow of bile from the liver. Bile is essential for digesting fats and removing waste products from the body. When bile flow is impaired, it can cause a buildup of bile acids in the liver, leading to liver damage. One specific form of this condition, […]
Cholestasis progressive intraheptic type 1, also known as Byler disease, is a rare genetic condition that affects the liver. It is caused by mutations in the ATP8B1 gene. This condition is characterized by impaired bile flow (cholestasis), which can lead to liver damage. Understanding the symptoms and undergoing genetic testing can be crucial for early […]
Cholestasis of pregnancy, also known as intrahepatic cholestasis of pregnancy (ICP), is a liver disorder that occurs in pregnant women. This condition can cause severe itching and increase the risk of fetal distress, preterm birth, and stillbirth. One of the genetic factors associated with this condition is mutations in the ABCB4 gene, which can lead […]
Understanding the symptoms and underlying genetic causes of certain diseases is crucial for effective diagnosis and management. Among these, Cholestasis of benign recurrent intrahepatic type 2, caused by mutations in the ABCB11 gene, is a condition that requires particular attention. DNA Labs UAE offers a comprehensive genetic test for this condition, aimed at providing accurate […]
In the rapidly evolving field of genetic testing, DNA Labs UAE stands at the forefront, offering a wide range of genetic tests designed to identify various genetic conditions and predispositions. Among these tests, the MT-RNR2 gene chloramphenicol resistance MT-RNR2 related genetic test is particularly significant due to its implications in antibiotic resistance and the potential […]
Chanarin-Dorfman Syndrome (CDS) is a rare genetic disorder that affects multiple organs and tissues across the body. It is primarily characterized by the accumulation of fats (lipids) in various cells, leading to a wide range of symptoms. The disorder is caused by mutations in the ABHD5 gene, which plays a crucial role in lipid metabolism. […]
Ceroid lipofuscinosis neuronal type 8, also known as CLN8 disease, is a rare genetic disorder that primarily affects the nervous system. It is part of a group of disorders known as neuronal ceroid lipofuscinoses (NCLs), which are characterized by the accumulation of lipofuscins – fatty substances – in the body’s tissues. These accumulations, particularly in […]
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.
