Albinism is a group of genetic conditions characterized by a reduction or complete lack of melanin pigment in the skin, hair, and eyes. Oculocutaneous albinism (OCA) is a form of albinism that affects the skin, hair, and eyes, and among its types, Oculocutaneous Type 4, caused by mutations in the SLC45A2 gene, stands out for […]
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 […]
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 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 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 disorders characterized by a lack or decrease in melanin production. The SLC24A5 gene plays a crucial role in the regulation of melanin synthesis, and mutations in this gene can lead to a specific form of albinism known as Oculocutaneous Albinism Type 4 (OCA4), which is a nonsyndromic type of […]
Adermatoglyphia, often dubbed as the “immigration delay disease,” is a rare genetic disorder characterized by the absence of fingerprints. This condition not only presents unique challenges in personal identification but also raises intriguing questions about genetic inheritance and variability. At DNA Labs UAE, we offer a comprehensive genetic test for the SMARCAD1 gene, which is […]
Symptoms of EOGT Gene Adams-Oliver Syndrome Type 4 Genetic Test Adams-Oliver Syndrome (AOS) is a rare genetic condition that can affect multiple parts of the body, including the skin, heart, and limbs. Among its various types, Type 4, caused by mutations in the EOGT gene, presents a unique set of challenges and symptoms for those […]
Adams-Oliver Syndrome (AOS) is a rare genetic condition that affects the development of the skin, skull, and limbs. A particularly uncommon subtype of this syndrome, known as Type 3, is linked to mutations in the RBPJ gene. Recognizing the symptoms associated with this genetic anomaly is crucial for early diagnosis and management. DNA Labs UAE […]
Adams-Oliver syndrome is a rare genetic condition that affects the development of the skin, skull, and limbs. Type 2 of this syndrome, specifically, is linked to mutations in the DOCK6 gene. Understanding the symptoms and the importance of genetic testing can be pivotal for early diagnosis and management of the condition. DNA Labs UAE offers […]
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.
