Bethlem myopathy, a rare genetic disorder, falls under the umbrella of collagen VI-related myopathies. This condition is primarily characterized by muscle weakness and joint stiffness (contractures), typically manifesting from early childhood, although symptoms can appear at any age. The COL6A2 gene plays a critical role in the development and functioning of muscles and connective tissues […]
Bethlem Myopathy Type 1 is a genetic condition that affects the connective tissue, primarily causing muscle weakness and joint stiffness. It is associated with mutations in the COL6A3 gene, which plays a crucial role in maintaining the structural integrity of muscle and skin tissues. As a leading genetic laboratory, DNA Labs UAE offers comprehensive testing […]
— Bethlem Myopathy Type 2 is a rare genetic condition that affects muscle development and function. This condition is caused by mutations in the COL12A1 gene, which plays a critical role in the strength and integrity of muscle and connective tissue. Recognizing the symptoms of Bethlem Myopathy Type 2 is crucial for early diagnosis and […]
Borjeson-Forssman-Lehmann Syndrome (BFLS) is a rare and complex genetic condition that affects many parts of the body. It is characterized by intellectual disability, obesity, seizures, gynecomastia (enlarged breast tissue in males), hypogonadism (a condition in which the sex glands produce little or no hormones), and distinctive facial features. The syndrome is caused by mutations in […]
Brody Myopathy is a rare genetic disorder that affects skeletal muscle function. It is characterized by muscle stiffness and difficulty relaxing muscles after contracting them, especially after exercise. This condition is caused by mutations in the ATP2A1 gene, which plays a crucial role in muscle relaxation by controlling calcium levels within muscle cells. Understanding the […]
The discovery of the MAOA gene and its link to Brunner syndrome has been a significant milestone in the field of genetics. This rare condition, also known as MAOA deficiency syndrome, has been the subject of extensive research. DNA Labs UAE is at the forefront of providing comprehensive genetic testing services, including the MAOA Gene […]
In the realm of medical genetics, the detection and understanding of specific gene mutations play a crucial role in diagnosing and managing various conditions. One such condition, Budd-Chiari Syndrome, has garnered attention due to its severe impact on liver function and overall health. This condition is often associated with mutations in the F5 gene, which […]
— Symptoms of ASPA Gene Canavan Disease Genetic Test Canavan Disease is a rare inherited disorder that affects the brain and the central nervous system’s ability to send and receive messages. It is caused by mutations in the ASPA gene, which leads to a deficiency of the enzyme aspartoacylase. This deficiency results in the accumulation […]
Symptoms of GYG2 Gene Autism Autism Spectrum Disorder (ASD) is a complex developmental condition that involves persistent challenges in social interaction, speech, and nonverbal communication, along with restricted/repetitive behaviors. The role of genetics in autism is significant, with numerous genes implicated in its development. One such gene is GYG2, which has recently been linked to […]
Autism spectrum disorder (ASD) is a complex developmental condition that involves persistent challenges in social interaction, speech and nonverbal communication, and restricted/repetitive behaviors. The signs of autism usually appear by age 2 or 3, but early diagnosis and intervention can lead to significant improvements. One of the breakthroughs in understanding the genetic basis of autism […]
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.
