Blogs

Osteopetrosis is a rare bone disorder characterized by the abnormal hardening and densification of bones, a condition that significantly impacts the overall quality of life of affected individuals. Among the various forms of osteopetrosis, the Autosomal Dominant Type 1, linked to mutations in the CLCN7 gene, presents a unique set of challenges and symptoms for […]

Osteopetrosis is a rare bone disorder characterized by the abnormal hardening of bones, leading to various health complications. Among the genetic causes of osteopetrosis, mutations in the SNX10 gene are associated with a severe form of the disease known as “Osteopetrosis of Infancy Malignant.” This condition not only affects bone density but also has implications […]

Osteopathia Striata with Cranial Sclerosis (OSCS) is a rare genetic disorder that affects the bones, leading to a combination of linear striations in the long bones and sclerosis of the skull. This condition is associated with mutations in the AMER1 gene, which plays a crucial role in bone development and growth. Understanding the symptoms of […]

Understanding the IL1RN Gene and Its Implications Osteomyelitis Sterile Multifocal with Periostitis and Pustulosis (OSMPP) is a rare genetic disorder that has puzzled medical professionals for years. However, advancements in genetic testing have shed light on the underlying cause of this condition, pinpointing the IL1RN gene as a key factor. At DNA Labs UAE, we […]

Understanding the intricacies of our genetic makeup can unlock answers to numerous health-related questions, including the likelihood of developing certain conditions. One such condition is Osteolysis Familial Expansile (OFE), a rare genetic disorder that can have significant implications on an individual’s bone health. At the heart of diagnosing this condition is the TNFRSF11A gene test, […]

Symptoms of PLOD2 Gene Osteogenesis Imperfecta with Congenital Joint Contractures Genetic Test Osteogenesis Imperfecta (OI), also known as brittle bone disease, is a genetic condition characterized by fragile bones that break easily. A less common subtype of this condition, associated with the PLOD2 gene, involves not just brittle bones but also congenital joint contractures, where […]

Osteogenesis Imperfecta (OI) is a group of genetic disorders that primarily affect the bones, leading to their increased fragility and susceptibility to fractures. Among the various types of OI, Type 9, linked to mutations in the PPIB gene, is a rare but significant form that requires careful diagnosis and management. DNA Labs UAE offers a […]

Osteogenesis Imperfecta (OI) is a group of genetic disorders that mainly affect the bones, making them fragile and more likely to break. Among the various types of OI, Type 8 is a rare form caused by mutations in the P3H1 gene. Understanding the symptoms and undergoing genetic testing can be crucial for individuals and families […]

Osteogenesis Imperfecta (OI), also known as brittle bone disease, is a group of genetic disorders that primarily affect the bones, leading to bones that break easily. Among the various types, Type 7, caused by mutations in the CRTAP gene, is one of the less common forms. Understanding the symptoms and genetic basis of Osteogenesis Imperfecta […]

Symptoms of SERPINF1 Gene Osteogenesis Imperfecta Type 6 Osteogenesis Imperfecta (OI) Type 6, a rare form of the genetic disorder known for causing fragile bones that break easily, is attributed to mutations in the SERPINF1 gene. Unlike other forms of OI that are primarily caused by collagen production issues, Type 6 involves a deficiency in […]