Symptoms of SLC35D1 Gene Schneckenbecken Dysplasia Genetic Test Schneckenbecken dysplasia is a rare and severe skeletal disorder that falls under the category of spondyloepiphyseal dysplasia. It is characterized by various skeletal anomalies that are present from birth. The SLC35D1 gene plays a crucial role in the development of this condition, and mutations in this gene […]
Schizencephaly is a rare developmental disorder characterized by abnormal slits or clefts in the cerebral hemispheres of the brain. One of the genes associated with this condition is the EMX2 gene, which plays a crucial role in brain development. Understanding the symptoms of schizencephaly and the significance of the EMX2 gene schizencephaly genetic test can […]
In the realm of genetics, understanding the intricate workings of our DNA can unlock answers to many medical mysteries. One such enigma is the Schinzel-Giedion Midface Retraction Syndrome, a condition linked to mutations in the SETBP1 gene. DNA Labs UAE stands at the forefront of genetic testing, offering comprehensive analysis for those seeking insights into […]
Symptoms of MAGEL2 Gene Schaaf-Yang Syndrome Genetic Test Schaaf-Yang syndrome is a complex genetic disorder that affects many parts of the body and is caused by mutations in the MAGEL2 gene. Recognizing the symptoms early on can significantly impact the management and treatment of the condition. DNA Labs UAE offers a comprehensive genetic test for […]
Understanding the complex nature of genetic disorders is pivotal for early diagnosis and effective management. Among these, a condition linked to mutations in the FGFR2 gene is of significant interest to medical researchers and clinicians. This condition is characterized by a unique combination of symptoms, including scaphocephaly, maxillary retrusion, and mental retardation. Recognizing these symptoms […]
Phocomelia Syndrome, also known as Roberts Syndrome (RBS) or SC Phocomelia Syndrome, is a rare genetic disorder characterized by severe prenatal and postnatal growth retardation, limb deficiencies, and facial anomalies. The syndrome is caused by mutations in the ESCO2 gene, which plays a crucial role in the cohesion of sister chromatids during cell division. Due […]
Saethre-Chotzen Syndrome (SCS) is a congenital condition characterized by craniosynostosis, which is the premature fusion of skull bones, leading to abnormalities in the shape of the head and face. This condition is caused by mutations in the TWIST1 gene, and understanding the symptoms can be crucial for early diagnosis and treatment. DNA Labs UAE offers […]
Saethre-Chotzen Syndrome (SCS) is a congenital condition, primarily characterized by craniosynostosis, which is the premature fusion of one or more cranial sutures leading to an abnormal head shape. It also involves facial asymmetries, ptosis (drooping of the upper eyelid), and limb abnormalities. This condition is caused by mutations in the FGFR2 (Fibroblast Growth Factor Receptor […]
Rubinstein-Taybi Syndrome (RTS) is a rare genetic disorder characterized by a wide range of physical, cognitive, and medical challenges. It is caused by mutations in the CREBBP and EP300 genes, which play crucial roles in the development of various tissues throughout the body. Understanding the symptoms and obtaining a definitive diagnosis through genetic testing is […]
— Rubinstein-Taybi Syndrome (RTS) is a rare genetic disorder that affects many parts of the body. Individuals with this condition often have distinctive facial features, broad thumbs and toes, short stature, and moderate to severe intellectual disability. The syndrome is primarily caused by mutations in the CREBBP gene, although mutations in the EP300 gene can […]
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.
