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Symptoms and Testing information for IDUA Gene Hurler Syndrome Genetic Test

Symptoms and Testing information for IDUA Gene Hurler Syndrome Genetic Test

In the realm of genetic testing, advancements have paved the way for the early detection and understanding of various genetic disorders, one of which is Hurler Syndrome. This condition, rooted in the IDUA gene, can have profound implications on an individual’s health and quality of life. DNA Labs UAE stands at the forefront of these […]

Symptoms and Testing information for HLCS Gene Holocarboxylase Synthetase Deficiency Genetic Test

Symptoms and Testing information for HLCS Gene Holocarboxylase Synthetase Deficiency Genetic Test

Holocarboxylase Synthetase (HLCS) deficiency is a rare genetic condition that affects the body’s ability to process certain proteins properly. This condition is caused by mutations in the HLCS gene, which plays a crucial role in the metabolism of several essential nutrients. Individuals with HLCS deficiency have difficulty converting certain forms of B-vitamins into their active […]

Symptoms and Testing information for F8 Gene Hemophilia A Genetic Test

Symptoms and Testing information for F8 Gene Hemophilia A Genetic Test

At DNA Labs UAE, we are committed to providing comprehensive genetic testing services that cater to a wide range of genetic conditions, including Hemophilia A. Hemophilia A is a serious genetic disorder that impairs the body’s ability to make blood clots, a process needed to stop bleeding. This condition is caused by a deficiency in […]

Symptoms and Testing information for GPI Gene Hemolytic Anemia Nonspherocytic Due to Glucose Phosphate Isomerase Deficiency Genetic Test

Symptoms and Testing information for GPI Gene Hemolytic Anemia Nonspherocytic Due to Glucose Phosphate Isomerase Deficiency Genetic Test

Understanding GPI Gene Hemolytic Anemia Nonspherocytic Due to Glucose Phosphate Isomerase Deficiency Glucose Phosphate Isomerase (GPI) deficiency is a rare genetic disorder that affects the way red blood cells function, leading to a form of hemolytic anemia known as GPI Gene Hemolytic Anemia Nonspherocytic. This condition is caused by mutations in the GPI gene, which […]

Symptoms and Testing information for SLC40A1 Gene Hemochromatosis Type 4 Genetic Test

Symptoms and Testing information for SLC40A1 Gene Hemochromatosis Type 4 Genetic Test

Hemochromatosis is a genetic condition characterized by excessive iron accumulation in the body, leading to various health issues. Type 4 Hemochromatosis, also known as Ferroportin Disease, is caused by mutations in the SLC40A1 gene. This particular type of hemochromatosis is autosomal dominant, meaning that inheriting a single copy of the mutated gene from one parent […]

Symptoms and Testing information for TFR2 Gene Hemochromatosis Type 3 Genetic Test

Symptoms and Testing information for TFR2 Gene Hemochromatosis Type 3 Genetic Test

Hemochromatosis is a genetic condition characterized by excessive absorption of iron from the diet, leading to a buildup of iron in the body’s organs. Among the different types of hemochromatosis, Type 3, caused by mutations in the TFR2 gene, is less common but significant. Understanding the symptoms and seeking timely genetic testing can be crucial […]

Symptoms and Testing information for HAMP Gene Hemochromatosis Type 2B Genetic Test

Symptoms and Testing information for HAMP Gene Hemochromatosis Type 2B Genetic Test

Understanding the implications and symptoms of genetic disorders is crucial in managing and mitigating their effects on individuals and families. One such condition that has garnered attention for its impact on iron metabolism is Hemochromatosis Type 2B, associated with mutations in the HAMP gene. This article delves into the symptoms of this genetic disorder and […]

Symptoms and Testing information for HJV Gene Hemochromatosis Type 2A Genetic Test

Symptoms and Testing information for HJV Gene Hemochromatosis Type 2A Genetic Test

Symptoms of HJV Gene Hemochromatosis Type 2A Genetic Test Hemochromatosis Type 2A, also known as Juvenile Hemochromatosis, is a rare genetic disorder caused by mutations in the HJV gene. This condition leads to an excessive accumulation of iron in the body, which can damage organs and lead to serious health issues. Understanding the symptoms of […]

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