Albinism is a group of genetic disorders characterized by a significant reduction in the amount or function of melanin, the pigment responsible for the color of the skin, hair, and eyes. One specific form, Oculocutaneous Albinism Type 1A (OCA1A), is caused by mutations in the TYR gene. This condition affects individuals from birth and presents […]
Albinism is a group of genetic conditions that result in little or no production of the pigment melanin, affecting the color of the skin, hair, and eyes. Among the various types, Oculocutaneous Albinism Type 1B (OCA1B) is specifically caused by mutations in the TYR gene. Understanding the symptoms and genetic basis of this condition is […]
Albinism is a group of genetic conditions characterized by a reduced amount or complete absence of pigment in the skin, hair, and eyes. Among the various types of albinism, Oculocutaneous Albinism Type 2 (OCA2) is one of the most common, particularly affecting individuals of African, African-American, and Native American descent. This condition is caused by […]
Albinism is a group of genetic disorders characterized by a reduction or complete lack of melanin pigment in the skin, hair, and eyes. Oculocutaneous albinism (OCA) is a type of albinism that affects the skin, hair, and eyes, and it has several subtypes. One of the subtypes, Oculocutaneous Type 3, also known as rufous or […]
Achondroplasia is a genetic disorder affecting bone growth, leading to dwarfism. This condition is primarily caused by mutations in the FGFR3 gene. Understanding the symptoms of achondroplasia and the significance of genetic testing can provide valuable insights for families and individuals potentially affected by this condition. DNA Labs UAE offers comprehensive genetic testing for achondroplasia […]
In the realm of genetic testing, advancements have made it possible to identify specific genes associated with various conditions. One such condition is Acne Inversa, also known as Hidradenitis Suppurativa, which can significantly affect an individual’s quality of life. At DNA Labs UAE, we offer a comprehensive genetic test for the PSEN1 Gene Acne Inversa […]
Acrodermatitis Enteropathica is a rare, autosomal recessive metabolic disorder that affects the way the body absorbs zinc. The condition is caused by mutations in the SLC39A4 gene, which plays a critical role in zinc absorption in the intestines. Without proper zinc absorption, individuals can suffer from a variety of symptoms, ranging from skin lesions to […]
Acrodysostosis 2, a rare genetic disorder, is caused by mutations in the PDE4D gene. This condition is characterized by a spectrum of physical and developmental symptoms that can significantly impact an individual’s quality of life. Understanding these symptoms is crucial for early diagnosis and management. DNA Labs UAE offers a comprehensive genetic test for Acrodysostosis […]
Acrofacial Dysostosis 1, Nager Type, is a rare genetic disorder that affects various parts of the body, including the face, hands, and arms. This condition is primarily caused by mutations in the SF3B4 gene, which plays a crucial role in the development of these body parts during embryonic growth. Recognizing the symptoms early on can […]
Acrokeratosis Verruciformis (AKV) is a rare genetic skin disorder, primarily characterized by the development of flat warts and lesions on the skin. This condition is closely associated with mutations in the ATP2A2 gene. Understanding the symptoms and undergoing genetic testing can be crucial for individuals suspecting they have AKV, as early detection can significantly aid […]
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.
