Popliteal Pterygium Syndrome (PPS) Type 1 is a rare genetic disorder that significantly impacts those affected and their families. At the core of this condition lies a mutation in the IRF6 gene, a crucial factor in the development of various body parts during embryonic growth. Understanding the symptoms of this condition is vital for early […]
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 […]
Symptoms of FGFR2 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. This condition also impacts the limbs and fingers. The FGFR2 gene plays a crucial role in the development of bones and […]
Orofaciodigital Syndrome Type 14 (OFD14), also known as C2CD3-related OFD, is a rare genetic disorder that affects the development of the oral cavity, facial features, and digits. This condition is part of a group of disorders known as orofaciodigital syndromes, each characterized by unique but overlapping symptoms. OFD14 is caused by mutations in the C2CD3 […]
Symptoms of TCTN3 Gene Orofaciodigital Syndrome Type 4 Genetic Test Orofaciodigital Syndrome Type 4 (OFD4), also known as Mohr-Majewski syndrome, is a rare genetic disorder that affects the development of the oral cavity, facial features, and digits. This condition is caused by mutations in the TCTN3 gene, which plays a critical role in the development […]
Symptoms of DDX59 Gene Orofaciodigital Syndrome Type 5 Genetic Test Orofaciodigital Syndrome Type 5 (OFD5), a rare genetic disorder, is marked by a distinctive pattern of physical features and abnormalities that affect the oral cavity, facial features, and digits. This condition is linked to mutations in the DDX59 gene, and understanding its symptoms is crucial […]
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.
