The Human Leukocyte Antigen (HLA) system is a crucial part of the immune system, playing a significant role in the body’s defense mechanisms against pathogens. Among its various components, the HLA-DR5 DRB1*1112 allele is of particular interest to medical researchers and clinicians due to its association with certain autoimmune diseases and conditions. Understanding the symptoms […]
Dysmorphology Diseases
Symptoms and Testing information for HLA – DR7 DRB1*07 Test
Symptoms of HLA – DR7 DRB1*07 Test The Human Leukocyte Antigen (HLA) system is a crucial part of the immune system, playing a significant role in the body’s defense against pathogens. The HLA – DR7 DRB1*07 allele is one specific marker within this system that has been associated with various autoimmune and inflammatory conditions. Understanding […]
Symptoms and Testing information for HLA – A2 A*02 Test
In the realm of genetic testing and diagnostics, understanding the implications of specific genetic markers is crucial for both patients and healthcare providers. One such marker that has garnered attention is the HLA-A2 A*02 allele. This allele is part of the Human Leukocyte Antigen (HLA) system, which plays a critical role in the immune system’s […]
Symptoms and Testing information for HLA – B15 B*15 Test
In the realm of genetic testing and diagnostics, the HLA – B15 B*15 Test stands out as a crucial tool for understanding an individual’s susceptibility to certain conditions and diseases. This test, offered by DNA Labs UAE, is a sophisticated analysis designed to identify the presence of the HLA-B*15 allele in an individual’s DNA. Understanding […]
Symptoms and Testing information for HLA – B22 B*22 Test
In the ever-evolving field of medical science, genetic testing has become a cornerstone for diagnosing and understanding various diseases and conditions. One such significant test is the HLA-B22 B*22 Test, which is crucial for identifying certain genetic markers that can affect an individual’s health. DNA Labs UAE is at the forefront of providing this essential […]
Symptoms and Testing information for HLA – Narcolepsy DRB115 DQB10602 DQA1*0102 Test
Narcolepsy is a chronic sleep disorder characterized by overwhelming daytime drowsiness and sudden attacks of sleep. People suffering from narcolepsy often find it difficult to stay awake for long periods, regardless of the circumstances. Narcolepsy can cause significant disruptions to a person’s daily life. It is associated with several genetic factors, one of which includes […]
Symptoms and Testing information for EPG5 Gene Vici Syndrome Genetic Test
Vici syndrome is a rare genetic disorder characterized by a spectrum of clinical manifestations, primarily affecting the brain, immune system, heart, skin, and eyes. It is caused by mutations in the EPG5 gene, which plays a crucial role in the autophagic process, essential for the degradation and recycling of cellular components. Recognizing the symptoms early […]
Symptoms and Testing information for ACTG2 Gene Visceral Myopathy Genetic Test
Visceral myopathy is a rare genetic disorder that affects the smooth muscles of the gastrointestinal tract, leading to a wide range of digestive problems. One of the genes associated with this condition is the ACTG2 gene. Mutations in this gene can lead to various symptoms that can significantly impact an individual’s quality of life. Understanding […]
Symptoms and Testing information for RAB3GAP1 Gene Warburg Micro Syndrome Type 1 Genetic Test
Warburg Micro Syndrome (WMS) is a rare genetic disorder characterized by a wide range of physical and developmental abnormalities. One of the genes associated with this condition is RAB3GAP1, and mutations in this gene lead to Warburg Micro Syndrome Type 1. At DNA Labs UAE, we offer a comprehensive genetic test for individuals suspected of […]
Symptoms and Testing information for RAB3GAP2 Gene Warburg Micro Syndrome Type 2 Genetic Test
Symptoms of RAB3GAP2 Gene Warburg Micro Syndrome Type 2 Genetic Test Warburg Micro Syndrome is a rare genetic disorder characterized by a wide spectrum of symptoms and physical anomalies. It is caused by mutations in the RAB3GAP2 gene, and the type 2 variant of the syndrome is specifically linked to this gene. This disorder is […]