Albinism is a group of genetic conditions characterized by a reduction or complete lack of melanin pigment in the skin, hair, and eyes. Oculocutaneous albinism (OCA) encompasses several types, with Type 7 being one of the rarest forms. This condition is primarily caused by mutations in the LRMDA gene. Recognizing the symptoms and understanding the […]
Alopecia Universalis is a condition that leads to the complete loss of hair on the scalp and body. It is an advanced form of alopecia areata, a condition that causes round patches of hair loss and can progress to total hair loss. The HR gene (Hairless gene) has been linked to this condition, and understanding […]
Amelogenesis Imperfecta (AI) is a hereditary condition characterized by the development of dental enamel that is abnormal in structure and appearance. Among the various types of AI, Type 1A is particularly notable for its severe impact on dental health. This condition is associated with mutations in the LAMB3 gene, which plays a crucial role in […]
Symptoms of ENAM Gene Amelogenesis Imperfecta Type 1B Amelogenesis Imperfecta (AI) is a congenital disorder affecting the enamel of teeth, leading to dental problems that are both cosmetic and functional in nature. Type 1B of this disorder, associated with mutations in the ENAM gene, is characterized by specific dental abnormalities. Understanding the symptoms of ENAM […]
Amelogenesis Imperfecta (AI) is a hereditary condition that affects the enamel of the teeth, making it thin, improperly formed, or absent altogether. This condition can lead to teeth that are discolored, sensitive, and prone to breakage or loss. Among the various types of AI, Type 1C, linked to mutations in the ENAM gene, presents unique […]
Amelogenesis Imperfecta (AI) is a congenital disorder that affects the structure and appearance of the enamel of teeth, leading to dental problems that can significantly impact an individual’s quality of life. Type 1E, associated with mutations in the AMELX gene, is a specific subtype of this condition. DNA Labs UAE offers a comprehensive genetic test […]
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 […]
Amelogenesis Imperfecta (AI) is a genetic condition that affects the development of the enamel, the hard, protective outer layer of the teeth. Type 1F, associated with mutations in the AMBN gene, is a specific subtype of this condition. DNA Labs UAE offers a comprehensive genetic test for this condition, providing invaluable information for affected individuals […]
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 […]
Amelogenesis Imperfecta (AI) is a congenital disorder that affects the enamel formation of teeth, leading to a variety of dental problems such as increased tooth decay, sensitivity, and aesthetic concerns. Type 1G, associated with mutations in the FAM20A gene, is a rare and specific subtype of this condition. Understanding the symptoms and the availability of […]
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.
