Olmsted Syndrome is a rare genetic condition that manifests through a variety of symptoms, significantly impacting the quality of life of those affected. It is primarily characterized by severe palmoplantar keratoderma (thickening of the skin on the palms of the hands and soles of the feet) and periorificial keratotic plaques (skin lesions around body orifices). […]
Symptoms of ALK Gene Neuroblastoma Type 3 Susceptibility to Familial Genetic Test Neuroblastoma is a type of cancer that most often affects children and is considered to be one of the most common tumors in infancy. It originates in the sympathetic nervous system, often in the adrenal glands, but can also develop in nerve tissues […]
Symptoms of MED12 Gene Opitz-Kaveggia Syndrome Genetic Test The MED12 gene plays a crucial role in the development of the nervous system and other bodily functions. Mutations in the MED12 gene can lead to a rare condition known as Opitz-Kaveggia Syndrome. This condition, also known as FG syndrome, affects many parts of the body and […]
Nicolaides-Baraitser Syndrome (NCBRS) is a rare genetic disorder characterized by distinctive facial features, sparse hair, prominent finger joints, and developmental delay. This condition is caused by mutations in the SMARCA2 gene, which plays a critical role in chromatin remodeling and thus impacts gene expression necessary for normal development. Recognizing the symptoms of NCBRS is crucial […]
In the realm of genetic diagnostics and personalized medicine, understanding the intricate details of our genetic makeup has become increasingly vital. One such area of focus is the study of the SUMO1 gene and its link to orofacial cleft type 10. At DNA Labs UAE, we specialize in providing comprehensive genetic testing services, including the […]
Nijmegen Breakage Syndrome (NBS) is a rare genetic disorder characterized by microcephaly (abnormally small head), a distinct facial appearance, growth retardation, an increased susceptibility to infections, and a higher risk of cancer, particularly lymphoma. This condition is caused by mutations in the NBN gene, which plays a crucial role in DNA repair and the maintenance […]
Understanding the intricacies of genetic conditions is crucial for timely diagnosis and appropriate management. Noonan Syndrome-like disorder with or without juvenile myelomonocytic leukemia, caused by mutations in the SHOC2 gene, is one such condition that necessitates comprehensive genetic analysis for accurate diagnosis. DNA Labs UAE stands at the forefront of genetic diagnostics, offering a specialized […]
Symptoms of PTPN11 Gene Noonan Syndrome Type 1 Genetic Test Noonan Syndrome is a genetic disorder that can affect various parts of the body. It is caused by mutations in several genes, including the PTPN11 gene. Noonan Syndrome Type 1, specifically associated with mutations in the PTPN11 gene, exhibits a range of clinical symptoms. Recognizing […]
Noonan Syndrome is a relatively common autosomal dominant congenital disorder that affects many parts of the body. It is characterized by unique facial features, short stature, heart defects, bleeding problems, skeletal malformations, and many other signs and symptoms. Noonan Syndrome Type 10, specifically caused by mutations in the LZTR1 gene, is one of the variants […]
Noonan Syndrome is a genetic disorder that affects various parts of the body. It is characterized by distinctive facial features, heart defects, developmental delays, and other physical abnormalities. One of the genes associated with Noonan Syndrome is the KRAS gene, which plays a crucial role in cell growth and development. Mutations in the KRAS gene […]
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.
