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 […]
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 […]
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 […]
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 […]
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 […]
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 […]
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 […]
— Hearing loss can significantly impact the quality of life, affecting everything from communication to social interactions. Among the various causes of hearing impairment, genetic factors play a crucial role. The MAP1A gene has been identified as one of the genetic contributors to hearing loss. Understanding the symptoms associated with MAP1A gene hearing loss and […]
Fazio-Londe disease, a rare and inherited neurological condition, is primarily characterized by progressive muscle weakness that typically begins in childhood. This disorder, linked to mutations in the SLC52A3 gene, affects the nervous system’s ability to communicate effectively with muscles, leading to significant motor function challenges. Recognizing the symptoms early and undergoing genetic testing can be […]
Deafness X-linked type 6, caused by mutations in the COL4A6 gene, is a rare genetic condition. This disorder, primarily affecting males due to its X-linked inheritance pattern, leads to varying degrees of hearing loss. Understanding the symptoms and undergoing genetic testing can be crucial for early diagnosis and management. DNA Labs UAE offers a comprehensive […]
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.
