Symptoms of HLA-B8 B*08 Test The HLA-B8 B*08 test is a specialized diagnostic procedure designed to identify the presence of the HLA-B8 allele in individuals. This allele is associated with various autoimmune and immune-mediated conditions. Recognizing the symptoms that may necessitate this test is crucial for timely diagnosis and management of related diseases. Here, we […]
Dysmorphology Diseases
Symptoms and Testing information for HLA – Cw6 C*06 Test
Symptoms of HLA – Cw6 C*06 Test Human Leukocyte Antigen (HLA) – Cw6 C*06 is a genetic marker associated with several autoimmune diseases, most notably psoriasis. Understanding the symptoms that necessitate the HLA – Cw6 C*06 test can be crucial for early detection and management of conditions linked to this genetic predisposition. DNA Labs UAE […]
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 FBN1 Gene Weill-Marchesani Syndrome Dominant Type 2 Genetic Test
Weill-Marchesani Syndrome (WMS) is a rare genetic disorder that affects the body’s connective tissue, leading to short stature, lens dislocation in the eye, and unique facial features among other symptoms. The syndrome has two main types, with Type 2 being associated with mutations in the FBN1 gene. Understanding the symptoms of FBN1 Gene Weill-Marchesani Syndrome […]
Symptoms and Testing information for WRN Gene Werner Syndrome Genetic Test
Werner syndrome, also known as adult progeria, is a rare, autosomal recessive disorder characterized by the appearance of premature aging. This condition is caused by mutations in the WRN gene, which plays a crucial role in DNA repair, replication, and recombination. The WRN gene Werner Syndrome Genetic Test is essential for individuals showing symptoms of […]
Symptoms and Testing information for KMT2A Gene Wiedemann-Steiner Syndrome Genetic Test
Wiedemann-Steiner Syndrome (WSS) is a rare genetic disorder characterized by a variety of physical, developmental, and intellectual challenges. This condition is caused by mutations in the KMT2A gene, which plays a significant role in the regulation of gene expression. Understanding the symptoms of WSS and the significance of genetic testing for this condition is crucial […]
Symptoms and Testing information for Chr. 7q11.23 Gene Williams-Beuren Syndrome Genetic Test
Williams-Beuren Syndrome (WBS) is a rare genetic disorder caused by a deletion of several genes on chromosome 7, specifically at the 7q11.23 locus. This complex condition is characterized by a range of medical and developmental issues, including cardiovascular disease, developmental delays, and distinctive facial features. Understanding the symptoms of Williams-Beuren Syndrome is crucial for early […]