Polymicrogyria (PMG) is a condition characterized by abnormal development of the brain before birth. The cerebral cortex, which is the brain’s outer layer responsible for many of its complex functions, develops too many small folds and fails to develop its normal grooves. One specific type of this condition, which involves the NR2E1 gene, leads to […]
Symptoms of MSX2 Gene Parietal Foramina Type 1 Parietal foramina type 1, caused by mutations in the MSX2 gene, is a rare genetic condition. This condition is characterized by the presence of one or more oval or circular defects in the parietal bones of the skull. These defects are due to incomplete bone formation (ossification) […]
Symptoms of LBR Gene Pelger-Huet Anomaly Genetic Test The Pelger-Huet anomaly is a rare, inherited condition that affects the white blood cells, specifically the neutrophils. It is caused by mutations in the LBR (lamin B receptor) gene. People with this condition have neutrophils that exhibit abnormal nuclear shapes, often described as hypolobulated, meaning the nuclei […]
Orofacial clefts are among the most common congenital anomalies, affecting numerous infants worldwide each year. These conditions can significantly impact an individual’s quality of life, affecting their ability to eat, speak, hear, and breathe properly. Advances in genetic testing have paved the way for early detection and intervention, offering hope to many families. Among these […]
Pelvic Organ Prolapse (POP) is a common condition that affects many women worldwide. It occurs when the muscles and tissues supporting the pelvic organs (the uterus, bladder, and rectum) become weak or loose, causing one or more of the pelvic organs to drop or press into or out of the vagina. Among the various factors […]
Orofacial clefts, comprising cleft lip and cleft palate anomalies, are among the most common congenital malformations, affecting approximately 1 in every 700 live births globally. These conditions not only impact the physical appearance but can also lead to significant functional challenges, including difficulties with feeding, speech, hearing, and dental development. Recent advancements in genetics have […]
Perlman Syndrome is a rare genetic disorder that can have serious implications for the health and development of affected individuals. It is characterized by overgrowth in infancy, renal dysplasia, and an increased risk for Wilms’ tumor and other malignancies. The DIS3L2 gene has been identified as a key factor in the development of Perlman Syndrome, […]
Orofacial clefts, which include cleft lip and cleft palate, are among the most common congenital anomalies worldwide. These conditions can significantly impact an individual’s quality of life, affecting not only their appearance but also their ability to speak, eat, and hear. Fortunately, advancements in genetics have paved the way for early detection and intervention, offering […]
Symptoms of FGFR1 Gene Pfeiffer Syndrome Genetic Test Pfeiffer Syndrome is a rare genetic disorder characterized by the premature fusion of certain skull bones (craniosynostosis), which affects the shape of the head and face. It is also known for affecting the limbs, particularly the fingers and toes. This condition is primarily caused by mutations in […]
DNA Labs UAE is at the forefront of genetic testing and diagnostics, offering a wide range of services designed to provide individuals with valuable insights into their genetic makeup. Among the various tests offered, the NECTIN1 Gene Orofacial Cleft Type 7 Genetic Test is a crucial diagnostic tool for families and individuals concerned about 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.
