Albinism is a group of genetic disorders characterized by a reduction or complete lack of melanin pigment in the skin, hair, and eyes. Among the various types of albinism, Oculocutaneous Albinism Type 4 (OCA4), caused by mutations in the SLC45A2 gene, is one of the less common forms. Understanding the symptoms and genetic basis of […]
At DNA Labs UAE, we are committed to providing advanced genetic testing services to help individuals and families gain valuable insights into their genetic makeup and potential health risks. Among our specialized tests, the CRYBB1 Gene Cataract Type 17 Multiple Types Genetic Test stands out for its importance in detecting a specific genetic predisposition to […]
Albinism is a group of genetic disorders characterized by a reduction or complete lack of melanin pigment in the skin, hair, and eyes. Among its various types, Oculocutaneous Albinism Type 5 (OCA5), associated with mutations in the C10ORF11 gene, is relatively less understood due to its recent discovery. Recognizing the symptoms associated with this genetic […]
DNA Labs UAE is at the forefront of genetic testing and diagnostics, offering a comprehensive range of services to help individuals understand their genetic makeup and its implications on their health. Among the various tests provided, the CRYBA4 Gene Cataract Type 23 Genetic Test is particularly noteworthy for individuals concerned about their ocular health and […]
Symptoms of PAX6 Gene Aniridia Genetic Test Aniridia is a rare genetic disorder characterized by the underdevelopment of the iris in the eye, which is the colored part surrounding the pupil. This condition is primarily associated with mutations in the PAX6 gene, a critical factor in eye development during the embryonic stage. Recognizing the symptoms […]
Symptoms of PITX3 Gene Anterior Segment Mesenchymal Dysgenesis Genetic Test Understanding the genetic basis of eye disorders can significantly improve the quality of life for those affected. Among these genetic conditions, anterior segment mesenchymal dysgenesis (ASMD) is a rare, inherited eye disorder that can lead to a range of symptoms affecting the anterior segment of […]
Bardet-Biedl Syndrome (BBS) is a complex genetic disorder that affects many parts of the body. Among the various types of this syndrome, Type 14, linked to mutations in the CEP290 gene, is one of the rare forms. Recognizing the symptoms of this condition is crucial for early diagnosis and management. DNA Labs UAE offers a […]
In the realm of genetic testing, advancements have paved the way for the identification and understanding of various genetic disorders that affect individuals worldwide. Among these is Bestrophinopathy, a condition associated with mutations in the BEST1 gene. DNA Labs UAE stands at the forefront of this scientific endeavor, offering comprehensive genetic testing services to diagnose […]
Symptoms of CYP4V2 Gene Bietti Crystalline Corneoretinal Dystrophy Bietti Crystalline Corneoretinal Dystrophy (BCCD) is a rare genetic condition that affects the retina, leading to progressive vision loss. This condition is caused by mutations in the CYP4V2 gene, which plays a crucial role in lipid metabolism within the eye. Recognizing the symptoms of BCCD is essential […]
The FOXL2 gene plays a critical role in the development of the eyelids and ovaries. Mutations in this gene can lead to a condition known as Blepharophimosis, Epicanthus Inversus, and Ptosis (BPES), a rare disorder that affects the eyes and, in some cases, fertility. Recognizing the symptoms of BPES is crucial for early diagnosis and […]
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.
