Understanding USH1C Gene Deafness Autosomal Recessive Type 18 Deafness, a condition affecting millions worldwide, can stem from various causes, including genetic factors. One such genetic cause is mutations in the USH1C gene, leading to a specific type of hearing loss known as Autosomal Recessive Type 18. This condition is not only characterized by profound deafness […]
The GJB2 gene, responsible for encoding the connexin 26 protein, plays a pivotal role in the functioning of the inner ear. Mutations in this gene can lead to a form of hearing loss known as Deafness Autosomal Recessive Type 1A (DFNB1A). This condition is characterized by a range of symptoms, making it crucial for individuals […]
In the realm of genetic diagnostics, understanding the intricacies of our genetic makeup is paramount for early detection, prevention, and management of inherited conditions. One such condition that has garnered attention in recent years is deafness autosomal dominant type 44, linked to mutations in the CCDC50 gene. DNA Labs UAE is at the forefront of […]
Understanding the nuances of genetic conditions is crucial for early detection and management. One such condition is deafness caused by mutations in the GJB6 gene, leading to Autosomal Recessive Deafness 1B. DNA Labs UAE offers a comprehensive genetic test for this condition, aimed at identifying the genetic markers associated with it. This article delves into […]
Deafness, a condition that significantly impacts an individual’s quality of life, can arise from various causes, including genetic factors. One such genetic cause is linked to mutations in the MYO1A gene, leading to a specific type of hearing loss known as Autosomal Dominant Deafness Type 48. Understanding the symptoms and available testing options for this […]
Understanding MYO7A Gene Deafness Autosomal Recessive Type 2 Deafness, a significant global health concern, affects countless individuals across different age groups. Among the various forms of hearing loss, genetic factors play a pivotal role, particularly in congenital and early-onset cases. One such genetic condition is linked to mutations in the MYO7A gene, leading to a […]
Deafness is a prevalent sensory impairment that affects millions of people worldwide. Among the various forms of hearing loss, genetic factors play a significant role. One such genetic condition is Deafness Autosomal Dominant Type 4B, linked to mutations in the CEACAM16 gene. Understanding the symptoms and undergoing genetic testing can be crucial for early diagnosis […]
Deafness is a condition that affects millions of people around the world, with various causes behind the impairment. Among these, genetic factors play a significant role, particularly in hereditary hearing loss. One such genetic condition is linked to the OTOA gene, leading to deafness autosomal recessive type 22. Understanding this condition, its symptoms, and the […]
The ACTG1 gene plays a crucial role in the function and structure of inner ear cells, which are essential for hearing. Mutations in this gene can lead to a condition known as Autosomal Dominant Deafness Type 20 (DFNA20), a form of hearing loss that presents in varying degrees of severity and can affect individuals from […]
The MYO6 Gene Deafness Autosomal Dominant Type 22 Genetic Test is a pivotal examination for individuals suspected of having or at risk of developing this specific type of hereditary hearing loss. Offered by DNA Labs UAE, this test provides crucial insights into the MYO6 gene, mutations of which are known to cause Autosomal Dominant Nonsyndromic […]
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.
