Symptoms of EOGT Gene Adams-Oliver Syndrome Type 4 Genetic Test Adams-Oliver Syndrome (AOS) is a rare genetic condition that can affect multiple parts of the body, including the skin, heart, and limbs. Among its various types, Type 4, caused by mutations in the EOGT gene, presents a unique set of challenges and symptoms for those […]
Adams-Oliver Syndrome (AOS) is a rare genetic condition that affects the development of the skin, skull, and limbs. A particularly uncommon subtype of this syndrome, known as Type 3, is linked to mutations in the RBPJ gene. Recognizing the symptoms associated with this genetic anomaly is crucial for early diagnosis and management. DNA Labs UAE […]
Adams-Oliver syndrome is a rare genetic condition that affects the development of the skin, skull, and limbs. Type 2 of this syndrome, specifically, is linked to mutations in the DOCK6 gene. Understanding the symptoms and the importance of genetic testing can be pivotal for early diagnosis and management of the condition. DNA Labs UAE offers […]
Adams-Oliver Syndrome (AOS) is a rare genetic disorder characterized by a spectrum of clinical features, including scalp defects, limb abnormalities, and, in some cases, heart defects and other problems. Type 1 AOS, associated with mutations in the ARHGAP31 gene, is one of the forms of this condition. Understanding the symptoms and genetic testing options, such […]
Acrokeratosis Verruciformis (AKV) is a rare genetic skin disorder, primarily characterized by the development of flat warts and lesions on the skin. This condition is closely associated with mutations in the ATP2A2 gene. Understanding the symptoms and undergoing genetic testing can be crucial for individuals suspecting they have AKV, as early detection can significantly aid […]
Acrofacial Dysostosis 1, Nager Type, is a rare genetic disorder that affects various parts of the body, including the face, hands, and arms. This condition is primarily caused by mutations in the SF3B4 gene, which plays a crucial role in the development of these body parts during embryonic growth. Recognizing the symptoms early on can […]
Acrodysostosis 2, a rare genetic disorder, is caused by mutations in the PDE4D gene. This condition is characterized by a spectrum of physical and developmental symptoms that can significantly impact an individual’s quality of life. Understanding these symptoms is crucial for early diagnosis and management. DNA Labs UAE offers a comprehensive genetic test for Acrodysostosis […]
Acrodermatitis Enteropathica is a rare, autosomal recessive metabolic disorder that affects the way the body absorbs zinc. The condition is caused by mutations in the SLC39A4 gene, which plays a critical role in zinc absorption in the intestines. Without proper zinc absorption, individuals can suffer from a variety of symptoms, ranging from skin lesions to […]
In the realm of genetic testing, advancements have made it possible to identify specific genes associated with various conditions. One such condition is Acne Inversa, also known as Hidradenitis Suppurativa, which can significantly affect an individual’s quality of life. At DNA Labs UAE, we offer a comprehensive genetic test for the PSEN1 Gene Acne Inversa […]
Achondroplasia is a genetic disorder affecting bone growth, leading to dwarfism. This condition is primarily caused by mutations in the FGFR3 gene. Understanding the symptoms of achondroplasia and the significance of genetic testing can provide valuable insights for families and individuals potentially affected by this condition. DNA Labs UAE offers comprehensive genetic testing for achondroplasia […]
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.
