Deafness is a significant global health concern, affecting millions of people worldwide. Among the various causes, genetic factors play a crucial role, especially in congenital or early onset hearing loss. One such genetic condition is deafness autosomal recessive type 48, attributed to mutations in the CIB2 gene. Understanding the symptoms and undergoing timely genetic testing […]
Deafness is a significant global health concern, affecting millions of individuals worldwide. Among the various causes of hearing loss, genetic factors play a crucial role. One such genetic condition is the MARVELD2 gene deafness, also known as autosomal recessive type 49. This condition is characterized by its mode of inheritance and its impact on an […]
Understanding the nuances of genetic conditions is pivotal in modern medicine, particularly when it comes to diagnosing and managing rare disorders. One such condition, associated with the COL11A2 gene, leads to a specific type of hearing loss known as Autosomal Recessive Deafness Type 53. This condition, while rare, highlights the importance of genetic testing in […]
Symptoms of PJVK Gene Deafness Autosomal Recessive Type 59 Genetic Test Deafness, autosomal recessive 59 (DFNB59), caused by mutations in the PJVK gene, is a form of non-syndromic hearing loss. Individuals with this condition often experience symptoms that can significantly impact their quality of life. Recognizing these symptoms early can lead to timely intervention and […]
Deafness is a condition that can significantly impact an individual’s quality of life, affecting their ability to communicate and interact with the world around them. Among the various causes of hearing loss, genetic factors play a crucial role. One such genetic condition is related to the RDX gene, leading to Autosomal Recessive Deafness Type 24 […]
Understanding the implications and symptoms of genetic conditions is crucial in the realm of medical science, particularly when it comes to conditions that affect our senses. One such condition is deafness caused by mutations in the TMIE gene, leading to Autosomal Recessive Type 63. At DNA Labs UAE, we offer a comprehensive genetic test for […]
In the realm of medical genetics, the discovery of gene-related conditions has paved the way for more precise and personalized treatment options. Among these conditions, hearing loss due to genetic mutations is a significant concern that affects millions worldwide. One such condition, caused by mutations in the GRXCR1 gene, leads to autosomal recessive deafness type […]
The SLC26A5 gene, also known as the prestin gene, plays a crucial role in the human body, particularly in the function of the cochlea in the inner ear. Mutations in this gene can lead to a form of hearing loss known as Autosomal Recessive Deafness Type 61 (DFNB61). This condition is characterized by the inability […]
Genetic testing has revolutionized the way we understand and manage hereditary conditions, offering insights that were previously unattainable. Among these advancements, the identification and analysis of the DIABLO gene, which is linked to Deafness Autosomal Dominant Type 64, stand out for its significance in understanding hearing loss. DNA Labs UAE is at the forefront of […]
In the realm of genetic diagnostics, the identification and understanding of specific genes that contribute to inherited conditions are paramount. One such gene, TBC1D24, has been linked to a form of deafness known as Autosomal Dominant Type 65. This condition, while rare, highlights the importance of genetic testing in providing crucial information for affected individuals […]
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.
