Albinism is a group of genetic conditions characterized by a reduction or complete lack of melanin pigment in the skin, hair, and eyes. Among the various types of albinism, Ocular Albinism Type I, also known as Nettleship-Falls Type, is a condition that primarily affects the eyes. This condition is linked to mutations in the GPR143 […]
Understanding the nuances of genetic disorders is crucial for early diagnosis and management. One such rare genetic condition is the Aland Island Eye Disease (AIED), primarily affecting males due to its X-linked inheritance pattern. This condition is caused by mutations in the CACNA1F gene, which plays a significant role in the normal functioning of the […]
Achromatopsia is a rare, inherited eye condition that significantly affects an individual’s vision, characterized primarily by a severe limitation in color discrimination, decreased vision, light sensitivity, and involuntary eye movements. Among the genes associated with this condition, mutations in the PDE6H gene are known to cause Achromatopsia Type 6. Understanding the symptoms of this genetic […]
Achromatopsia, a rare genetic condition affecting approximately 1 in 30,000 individuals worldwide, is characterized by a significant reduction or complete absence of color vision. Among the genes implicated in this condition, the GNAT2 gene is noteworthy for its role in Achromatopsia Type 4. DNA Labs UAE is at the forefront of genetic testing for this […]
Understanding Achromatopsia Type 3 Achromatopsia Type 3 is a rare genetic condition that significantly affects an individual’s vision, primarily characterized by a complete or partial absence of color vision, light sensitivity, and visual acuity limitations. This condition stems from mutations in the CNGB3 gene, which plays a crucial role in the normal functioning of cone […]
Achromatopsia is a rare, inherited eye condition that severely limits a person’s ability to see color, perceive fine detail, and tolerate bright light. Among the genetic variants that cause achromatopsia, mutations in the CNGA3 gene are responsible for what is known as Achromatopsia Type 2. Understanding the symptoms of this condition is crucial for early […]
In the realm of genetic testing and diagnostics, the Chromosomal Microarray (CMA) 750K High Resolution Test stands out as a revolutionary tool. Offered by DNA Labs UAE, this comprehensive test is designed to detect various chromosomal abnormalities that can be linked to numerous genetic disorders. With an aim to provide in-depth insights into one’s genetic […]
In the realm of personalized medicine and advanced diagnostics, the Oncopro BRAF Rapid Test stands out as a significant advancement, particularly in the field of oncology. Offered by DNA Labs UAE, this test represents a leap forward in the early detection and treatment planning for various cancers. The BRAF gene mutation is a critical biomarker […]
DNA Labs UAE is at the forefront of genetic and immunological diagnostics, offering a wide range of tests and analyses to help patients and healthcare providers understand complex genetic information. One of the critical tests provided by DNA Labs UAE is the HLA Single Antigen Bead Assay for Class I IgG Antibodies DSA-SAB Class I […]
Growth Hormone Releasing Hormone (GHRH) plays a pivotal role in regulating human growth and development. It stimulates the pituitary gland to release growth hormone (GH), which is crucial for normal physical growth in children and metabolic functions in adults. An imbalance in GHRH can lead to various health issues, necessitating accurate diagnostic procedures. DNA Labs […]
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.
