Frontonasal dysplasia type 2, caused by mutations in the ALX4 gene, is a rare genetic disorder. This condition is characterized by a range of physical malformations affecting the head and face, most notably the forehead and nose. Understanding the symptoms and undergoing genetic testing can be crucial for diagnosis, management, and family planning. DNA Labs […]
Ellis-van Creveld syndrome (EVC) is a rare genetic disorder that affects bone growth, leading to skeletal dysplasia among other symptoms. Understanding the signs and symptoms of this condition is crucial for early diagnosis and management. DNA Labs UAE offers a comprehensive genetic test for EVC, providing a vital tool for families seeking answers. Symptoms of […]
Ellis-van Creveld syndrome (EvC) is a rare genetic disorder that affects bone growth among other physical manifestations. This condition, inherited in an autosomal recessive manner, primarily involves the shortening of the forearms and lower legs (a condition known as mesomelic dwarfism), polydactyly (extra fingers or toes), and abnormalities in the fingernails and teeth. The EVC2 […]
Understanding the symptoms and genetic underpinnings of complex medical conditions is crucial for effective diagnosis and treatment. One such condition, Epiphyseal Dysplasia Multiple with Myopia and Deafness, is linked to mutations in the COL2A1 gene. DNA Labs UAE offers a comprehensive genetic test for this condition, which is essential for individuals experiencing symptoms or with […]
Faciogenital dysplasia, also known as Aarskog-Scott syndrome, is a rare genetic disorder that primarily affects the development of the face, hands, and genitals. It is caused by mutations in the FGD1 gene. Understanding the symptoms of this condition is crucial for early diagnosis and management. DNA Labs UAE offers a comprehensive genetic test for the […]
Symptoms of ERCC4 Gene Fanconi Anemia Complementation Group Q Genetic Test Fanconi Anemia (FA) is a rare, inherited blood disorder that leads to bone marrow failure. The ERCC4 gene, also known as FANCQ, has been identified as one of the genes associated with this condition. Individuals with mutations in the ERCC4 gene may develop Fanconi […]
Understanding CANT1 Gene Desbuquois Dysplasia Type 1 Desbuquois Dysplasia is a rare genetic disorder that affects bone development in individuals. It is primarily caused by mutations in the CANT1 gene. This condition is characterized by a variety of symptoms that can significantly impact the quality of life of those affected. Recognizing the symptoms early on […]
Understanding Feingold Syndrome and the Role of MYCN Gene Feingold syndrome is a rare genetic disorder that affects many parts of the body. It is characterized by specific physical anomalies and developmental delays. The condition is primarily caused by mutations in the MYCN gene, a critical component in the development of various tissues in the […]
Desbuquois Dysplasia is a rare genetic disorder that affects bone development in individuals. It is characterized by a variety of symptoms that can impact a person’s quality of life significantly. Among the genes associated with this condition, mutations in the XYLT1 gene have been identified to cause Desbuquois Dysplasia Type 2. Understanding the symptoms and […]
Understanding the genetic underpinnings of various conditions is a crucial step towards providing targeted and effective treatments. Among these genetic conditions is the Fetal Akinesia Deformation Sequence (FADS), which has been linked to mutations in the DOK7 gene. This article aims to shed light on the symptoms associated with DOK7 gene mutations and the importance […]
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.
