Hyperlipoproteinemia Type 1, also known as Familial Lipoprotein Lipase Deficiency (LPLD), is a rare genetic disorder that affects the body’s ability to break down fats, leading to a significant increase in blood triglyceride levels. This condition is caused by mutations in the LPL gene, which encodes the lipoprotein lipase enzyme, pivotal in the metabolism of […]
Metabolic Disorders
Symptoms and Testing information for LDLR Gene Hypercholesterolemia Due to LDL-Receptor-Disorder Autosomal Dominant Genetic Test
In the realm of genetic testing, understanding the intricacies of our genetic makeup has never been more accessible. Among the myriad of genetic conditions that can be identified through advanced testing, Hypercholesterolemia due to LDL-Receptor-Disorder (LDLR Gene Hypercholesterolemia) stands out for its significant impact on cardiovascular health. DNA Labs UAE, a leading genetic laboratory, offers […]
Symptoms and Testing information for AASS Gene Hyperlysinemia Type 1 Genetic Test
Hyperlysinemia Type 1 is a rare genetic disorder that affects the way the body metabolizes the amino acid lysine. It is caused by mutations in the AASS gene, which leads to an accumulation of lysine in the blood. This condition can have various symptoms and is often diagnosed through genetic testing. DNA Labs UAE offers […]
Symptoms and Testing information for APOB Gene Hypercholesterolemia Type B Autosomal Dominant Genetic Test
Hypercholesterolemia, specifically Type B Autosomal Dominant Hypercholesterolemia, is a condition that can have significant implications on an individual’s health, particularly cardiovascular health. This condition is often linked to the APOB gene, which plays a crucial role in lipid metabolism. Understanding the symptoms and undergoing genetic testing for this condition is vital for early detection and […]
Symptoms and Testing information for SLC30A10 Gene Hypermanganesemia with Dystonia Polycythemia and Cirrhosis Genetic Test
Understanding SLC30A10 Gene Hypermanganesemia with Dystonia, Polycythemia, and Cirrhosis SLC30A10 gene hypermanganesemia with dystonia, polycythemia, and cirrhosis is a rare genetic disorder that affects various systems in the body, leading to a wide range of symptoms. This condition is caused by mutations in the SLC30A10 gene, which plays a crucial role in regulating manganese levels […]
Symptoms and Testing information for EPHX2 Gene Hypercholesterolemia Familial Due to LDLR Defect Modifier of Genetic Test
In the intricate landscape of genetic disorders, Familial Hypercholesterolemia (FH) stands out due to its significant impact on cardiovascular health. This condition, primarily caused by mutations in the LDL receptor gene (LDLR), leads to elevated levels of low-density lipoprotein cholesterol (LDL-C) in the blood, increasing the risk of heart disease. However, recent studies have illuminated […]
Symptoms and Testing information for ADK Gene Hypermethioninemia Due to Adenosine Kinase Deficiency Genetic Test
In the realm of genetic testing, advancements have paved the way for identifying a myriad of genetic disorders that were once difficult to diagnose. Among these conditions, ADK Gene Hypermethioninemia due to Adenosine Kinase Deficiency presents a unique challenge for both patients and medical professionals. This genetic disorder, although rare, can have significant implications on […]
Symptoms and Testing information for APOA2 Gene Hypercholesterolemia Familial Modifier of Genetic Test
— Understanding APOA2 Gene Hypercholesterolemia Familial Modifier Hypercholesterolemia, a condition characterized by very high levels of cholesterol in the blood, is a major risk factor for coronary heart disease. While diet, lifestyle, and general health are significant contributors to this condition, genetics also plays a crucial role. One such genetic factor is the APOA2 gene, […]
Symptoms and Testing information for SLC25A15 Gene Hyperornithinemia- Hyperammonemia – Homocitrullinuria Syndrome Genetic Test
Hyperornithinemia-Hyperammonemia-Homocitrullinuria (HHH) Syndrome is a rare but serious genetic disorder that affects the body’s ability to process and eliminate ammonia. This condition is caused by mutations in the SLC25A15 gene, which plays a critical role in the urea cycle and the metabolism of amino acids. Individuals with HHH Syndrome may experience a range of symptoms […]
Symptoms and Testing information for ITIH4 Gene Hypercholesterolemia Susceptibility to Genetic Test
In the intricate tapestry of human genetics, the ITIH4 gene emerges as a significant marker for predicting the risk of hypercholesterolemia, a condition characterized by high levels of cholesterol in the blood. This condition is a primary risk factor for cardiovascular diseases, including heart attack and stroke, making early detection and management crucial. DNA Labs […]