Camurati-Engelmann Disease (CED), also known as progressive diaphyseal dysplasia, is a rare genetic disorder that primarily affects the bones. Individuals with this condition often experience bone pain, muscle weakness, and a waddling gait, among other symptoms. The disease is caused by mutations in the TGFB1 gene, which plays a crucial role in bone development and […]
Auriculocondylar Syndrome Type 2 (ACS2) is a rare genetic disorder that affects the development of the ear, mandible (jawbone), and in some cases, the heart. This condition is primarily caused by mutations in the PLCB4 gene, which plays a crucial role in the development of these structures. Recognizing the symptoms of ACS2 is vital for […]
Understanding Bjornstad Syndrome Bjornstad Syndrome is a rare genetic disorder that is characterized by two primary symptoms: sensorineural hearing loss and pili torti, a condition where the hair is brittle, coarse, and lacks pigmentation, leading to early hair loss. This disorder is caused by mutations in the BCS1L gene, which plays a crucial role in […]
Symptoms of PITX2 Gene Axenfeld-Rieger Syndrome Type 1 Genetic Test Axenfeld-Rieger Syndrome (ARS) is a rare genetic disorder that affects the development of the eyes, teeth, and abdominal region. It is primarily associated with mutations in the PITX2 gene, which plays a crucial role in the early development of these areas. Recognizing the symptoms of […]
Blau syndrome is a rare genetic disorder that is often characterized by a triad of symptoms: granulomatous arthritis, uveitis, and dermatitis. It is an autosomal dominant condition, meaning that only one copy of the mutated gene is necessary for the manifestation of the disorder. The gene associated with Blau syndrome is NOD2, located on chromosome […]
Axenfeld-Rieger Syndrome (ARS) is a rare genetic disorder that affects various parts of the body, including the eyes, teeth, and facial structure. Type 3 ARS, specifically linked to mutations in the FOXC1 gene, is one of the subtypes of this condition. Understanding the symptoms and undergoing genetic testing can be crucial for early diagnosis and […]
Bohring-Opitz Syndrome (BOS) is a rare genetic disorder that is primarily characterized by severe developmental delays, distinctive facial features, and various physical abnormalities. The syndrome is caused by mutations in the ASXL1 gene, which plays a crucial role in the regulation of gene expression. Recognizing the symptoms of Bohring-Opitz Syndrome is essential for early diagnosis […]
— Bainbridge-Ropers Syndrome (BRS) is a rare genetic disorder that affects multiple aspects of a patient’s health and development. It is caused by mutations in the ASXL3 gene, which plays a crucial role in the regulation of gene expression. DNA Labs UAE offers a comprehensive genetic test for those who suspect they or their family […]
Understanding the complexities of genetic conditions is crucial for early diagnosis and management. Among these, the mutation of the OCLN gene leading to Band-Like Calcification with Simplified Gyration and Polymicrogyria (BLC-SGP) is a rare but significant disorder that affects the brain’s development. DNA Labs UAE offers a comprehensive genetic test for this condition, providing invaluable […]
At DNA Labs UAE, we understand the complexities and concerns that come with genetic conditions, and we are committed to providing our clients with accurate, comprehensive genetic testing services. One such service we offer is the ACTB Gene Baraitser-Winter Syndrome Type 1 Genetic Test. This detailed examination is crucial for individuals suspecting they might have […]
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.
