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 […]
Ear Nose Throat Diseases
Symptoms and Testing information for GJB2 Gene Keratoderma Palmoplantar with Deafness Genetic Test
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 […]
Symptoms and Testing information for GJB2 Gene Knuckle Pads and Leukonychia Sensorineural Deafness Genetic Test
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 and Testing information for COL11A1 Gene Marshall Syndrome Genetic Test
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 […]
Symptoms and Testing information for TRMU Gene Mitochondrial Modifier of Deafness Genetic Test
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 and Testing information for TIMM8A Gene Opticoacoustic Nerve Atrophy with Dementia Genetic Test
In the realm of genetic diagnostics, the pursuit of understanding and identifying the root causes of complex conditions has led to the development of sophisticated genetic tests. One such pivotal test is the TIMM8A Gene Opticoacoustic Nerve Atrophy with Dementia Genetic Test, offered by DNA Labs UAE. This specific examination is designed to detect mutations […]
Symptoms and Testing information for FLNA Gene Otopaladigital Syndrome Type 1 Genetic Test
Otopalatodigital syndrome type 1 (OPD1) is a rare genetic disorder that affects bone growth and development, leading to skeletal abnormalities and a range of other potential physical issues. This condition is caused by mutations in the FLNA gene, which plays a critical role in cell structure and movement. Understanding the symptoms of this disorder is […]
Symptoms and Testing information for FLNA Gene Otopaladigital Syndrome Type 2 Genetic Test
Understanding the symptoms of FLNA Gene Otopaladigital Syndrome Type 2 and the importance of genetic testing is crucial for early diagnosis and management of the condition. FLNA Gene Otopaladigital Syndrome Type 2 is a rare genetic disorder that can affect multiple systems within the body, leading to a range of symptoms that may impact an […]
Symptoms and Testing information for TMC1 Gene Deafness Autosomal Recessive Type 7 Genetic Test
Deafness, particularly when it stems from genetic origins, can profoundly impact individuals and their families. One such genetic condition is linked to mutations in the TMC1 gene, leading to autosomal recessive deafness type 7. Understanding this condition, recognizing its symptoms, and undergoing genetic testing can provide critical insights for affected individuals and their families. DNA […]
Symptoms and Testing information for POU3F4 Gene Deafness X-Linked Type 2 Genetic Test
In the realm of genetic testing and diagnosis, understanding the nuances of specific genetic conditions is paramount for early detection and management. One such condition that has garnered attention is the POU3F4 gene-related deafness, specifically X-linked type 2. This condition, while not as widely recognized as other forms of hearing impairment, presents a unique set […]