Symptoms of OCA2 Gene Albinism Oculocutaneous Type 2 Oculocutaneous albinism type 2 (OCA2), caused by mutations in the OCA2 gene, is a genetic condition characterized by reduced pigmentation in the hair, skin, and eyes. This form of albinism, while affecting melanin production, varies significantly in terms of its presentation among individuals, with symptoms ranging from […]

Albinism is a group of genetic disorders characterized by 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. This type of albinism not only affects the pigmentation but also […]

Albinism is a group of genetic disorders characterized by a lack or decrease in melanin production. Melanin is the pigment responsible for the color of the skin, hair, and eyes. Among the different types of albinism, Oculocutaneous Albinism Type 1A (OCA1A) is one of the most severe forms, caused by mutations in the TYR gene. […]

Albinism is a genetic condition that affects the production of melanin, the pigment that colors our skin, hair, and eyes. Among the various types of albinism, Oculocutaneous Albinism (OCA) is one that not only impacts the appearance of an individual’s skin and hair but also their vision. A specific form of this condition, linked to […]

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 […]