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 […]
At DNA Labs UAE, we are dedicated to providing comprehensive genetic testing services to help individuals and families gain crucial insights into their genetic makeup, enabling them to make informed health and lifestyle decisions. Among our specialized offerings is the MASP1 Gene 3MC Syndrome Type 1 Genetic Test, a critical tool for diagnosing a rare […]
3MC syndrome is a rare genetic condition that affects various parts of the body. The term “3MC” stands for the three conditions it was initially thought to encompass: Mingarelli, Malpuech, Michels, and Carnevale syndromes. However, it is now understood that these conditions represent a spectrum of a single disorder. 3MC syndrome type 2 is specifically […]
Understanding the genetic makeup of individuals has become a cornerstone in modern medical diagnostics and treatment planning. Among the myriad of genetic conditions that have been identified, achondrogenesis Type 1A, linked to mutations in the TRIP11 gene, stands out due to its rarity and severity. DNA Labs UAE, a leading institution in genetic testing, offers […]
At DNA Labs UAE, we understand the critical importance of accurate genetic testing for families and individuals facing the possibility of genetic conditions. One such rare but severe genetic disorder is Achondrogenesis Type 1B, which is caused by mutations in the SLC26A2 gene. This condition affects the development of bones and cartilage, leading to a […]
Achondrogenesis Type 2, caused by mutations in the COL2A1 gene, is a severe disorder that affects the development of bones and cartilage in the body. This rare genetic condition is part of a group of disorders known as chondrodysplasias, which lead to skeletal abnormalities through the disruption of the normal process of bone growth. Understanding […]
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.
