Symptoms of TMCO1 Gene Craniofacial Dysmorphism Skeletal Anomalies and Mental Retardation Syndrome The TMCO1 Gene Craniofacial Dysmorphism Skeletal Anomalies and Mental Retardation Syndrome is a complex genetic condition that affects various aspects of physical and cognitive development. This syndrome is characterized by a unique set of symptoms that can vary in severity among individuals. Recognizing […]
Cornelia de Lange Syndrome (CdLS) is a rare genetic disorder that can affect multiple parts of the body. It is characterized by distinctive facial features, growth delays, intellectual disability, and limb defects. Among the various genes associated with CdLS, mutations in the HDAC8 gene lead to a specific subtype known as Cornelia de Lange Syndrome […]
Cornelia de Lange Syndrome (CdLS) is a rare genetic disorder that can affect multiple parts of the body. This condition is known for its distinctive facial features, growth delays, intellectual disability, and limb defects. Among the genes associated with CdLS, the RAD21 gene plays a critical role. Mutations in the RAD21 gene can lead to […]
Cornelia de Lange Syndrome (CdLS) is a rare genetic disorder that can affect multiple parts of the body. It is characterized by distinctive facial features, growth delays, intellectual disability, and limb defects. Among the genes associated with this condition, mutations in the SMC3 gene have been identified to cause a specific subtype of the syndrome, […]
Cornelia de Lange Syndrome (CdLS) is a rare genetic disorder that affects various parts of the body. Among the genes associated with this syndrome, mutations in the SMC1A gene lead to a specific subtype known as Cornelia de Lange Syndrome Type 2. Recognizing the symptoms associated with this condition is crucial for early diagnosis and […]
Symptoms of NIPBL Gene Cornelia de Lange Syndrome Type 1 Genetic Test Cornelia de Lange Syndrome (CdLS) Type 1 is a rare genetic disorder that affects various parts of the body. It is primarily characterized by delayed growth and development, intellectual disability, limb defects, and distinctive facial features. The NIPBL gene plays a crucial role […]
Understanding the intricacies of our genetic makeup has become increasingly important in diagnosing, treating, and managing various genetic disorders. Among these, FBN2 Gene Contractural Arachnodactyly, also known as Beals Syndrome, is a condition that has garnered attention due to its impact on individuals from a young age. DNA Labs UAE offers a comprehensive genetic test […]
At DNA Labs UAE, we are committed to providing our clients with comprehensive and accurate genetic testing services to diagnose a wide range of conditions, including immunodeficiencies. One such condition is the X-linked combined immunodeficiency caused by mutations in the IL2RG gene. This condition, while rare, can have significant impacts on the health and well-being […]
DNA Labs UAE is at the forefront of genetic testing and diagnostics, offering a wide array of tests to diagnose genetic conditions. Among these, the RAG2 Gene Combined Immunodeficiency B Cell-Negative T Cell-Negative NK Cell Positive Genetic Test stands out for its critical importance in identifying a rare but severe immunodeficiency disorder. This condition, often […]
The RAG2 gene plays a crucial role in the immune system, facilitating the development of T and B cells, which are essential for the body’s defense against pathogens. A mutation in this gene can lead to a complex condition known as Combined Cellular and Humoral Immune Defects with Granulomas. This rare genetic disorder impacts the […]
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.
