Primary Ciliary Dyskinesia (PCD) is a rare genetic disorder that affects the cilia, which are tiny, hair-like structures that line the airways, reproductive system, and other parts of the body. These cilia play a crucial role in moving mucus and other substances out of the airways, helping to protect the lungs from infection and inflammation. […]
Primary Ciliary Dyskinesia (PCD) is a rare genetic disorder that affects the cilia, tiny hair-like structures that line the airways, ears, and other parts of the body. These cilia play a pivotal role in moving mucus and other substances through the airways, protecting the lungs from infections and debris. One of the genes associated with […]
Understanding the implications and symptoms of genetic conditions is crucial for early diagnosis and effective management. Among these conditions is Primary Ciliary Dyskinesia (PCD), specifically Type 25, linked to the DYX1C1 gene. This article explores the symptoms associated with this condition and provides information on the genetic testing available through DNA Labs UAE for its […]
Primary Ciliary Dyskinesia (PCD) is a rare genetic disorder that affects the cilia, the tiny hair-like structures that line the airways, ears, and other parts of the body. The CFAP298 gene has been identified as one of the genetic contributors to PCD, specifically known as Primary Ciliary Dyskinesia Type 26. Understanding the symptoms associated with […]
Primary Ciliary Dyskinesia (PCD) is a rare genetic disorder that affects the cilia, the tiny hair-like structures that line the airways, ears, and other parts of the body. These cilia play a crucial role in moving mucus and other materials out of the airways, ears, and sinuses. When they are dysfunctional due to genetic mutations, […]
Symptoms of SPAG1 Gene Primary Ciliary Dyskinesia Type 28 Genetic Test Primary Ciliary Dyskinesia (PCD) is a rare genetic disorder that affects the cilia, the microscopic, hair-like structures that line the airways, ears, and other parts of the body. One specific subtype of this condition, known as Type 28, is caused by mutations in the […]
Primary Ciliary Dyskinesia (PCD) is a rare genetic disorder that affects the cilia, the microscopic, hair-like structures that line the airways, ears, and other parts of the body. These cilia play a crucial role in moving mucus and other substances out of the respiratory tract and other areas. When cilia do not function properly due […]
DNA Labs UAE is at the forefront of genetic testing and diagnostics, offering a comprehensive range of tests aimed at identifying various genetic conditions. One such test is for the DNAH5 Gene, associated with Primary Ciliary Dyskinesia Type 3 (PCD). This condition is rare and can affect individuals from a very young age, leading to […]
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 […]
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.
