Understanding the symptoms of MYH7B gene hearing loss is crucial for early detection and intervention. The MYH7B gene, located on chromosome 20, plays a significant role in the development and function of the inner ear structures that process sound. Mutations in this gene can lead to various types of hearing impairment, ranging from mild to […]
DNA Labs UAE is at the forefront of genetic testing, offering a comprehensive range of services designed to provide insights into various genetic conditions. One such condition that DNA Labs UAE can help diagnose is Primary Ciliary Dyskinesia (PCD), specifically Type 13, which is linked to mutations in the DNAAF1 gene. Understanding the symptoms of […]
Symptoms of PEX1 Gene Heimler Syndrome Type 1 Genetic Test Heimler Syndrome is a rare genetic disorder that is passed down through families in an autosomal recessive pattern. It is primarily characterized by sensorineural hearing loss, dental anomalies, nail abnormalities, and occasionally, visual impairment due to retinal dystrophy. The condition is linked to mutations in […]
Keratitis Ichthyosis Deafness (KID) Syndrome is a rare genetic disorder that affects the skin, eyes, and hearing. It is caused by mutations in the GJB2 gene, which encodes for the protein connexin 26, essential for the proper functioning of cells in the skin, inner ear, and eyes. This disorder falls under the category of autosomal […]
At DNA Labs UAE, we are committed to providing advanced genetic testing services to help individuals understand their genetic predispositions to various conditions. One such condition is the Keratoderma Palmoplantar with Deafness, associated with mutations in the GJB2 gene. This article will explore the symptoms associated with this condition and the importance of the GJB2 […]
In the quest to understand the intricate web of genetics that dictates various conditions in humans, the GJB2 gene has come under significant scrutiny. This gene, primarily associated with sensorineural deafness, has also been linked to other physical manifestations, including knuckle pads and leukonychia (white nails). Understanding these symptoms and their genetic underpinnings is crucial […]
Symptoms of COL11A1 Gene Marshall Syndrome Genetic Test Marshall Syndrome, a genetic disorder caused by mutations in the COL11A1 gene, presents a variety of symptoms that can significantly impact an individual’s quality of life. Recognizing these symptoms early can lead to timely intervention and management. DNA Labs UAE offers a comprehensive genetic test for Marshall […]
Understanding the symptoms of genetic conditions is crucial for early diagnosis and management. One such condition involves mutations in the TRMU gene, which can play a significant role in hearing loss. At DNA Labs UAE, we offer a comprehensive TRMU Gene Mitochondrial Modifier of Deafness Genetic Test, designed to detect mutations in the TRMU gene […]
Understanding the complex nature of genetic disorders is crucial for early diagnosis and treatment. Among these disorders, the BCAP31 gene mutation stands out due to its rare but significant impact on affected individuals. This mutation is linked to a severe condition characterized by deafness, dystonia, and cerebral hypomyelination, and it is inherited in an X-linked […]
Deafness can profoundly impact an individual’s quality of life, affecting their communication, education, and social interactions. Among the various causes of hearing loss, genetic factors play a significant role. The MT-RNR1 gene, associated with nonsyndromic sensorineural mitochondrial genetic deafness, is one such genetic factor. DNA Labs UAE offers a comprehensive genetic test for this condition, […]
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.
