Symptoms of GNE Gene Inclusion Body Myopathy Genetic Test GNE Gene Inclusion Body Myopathy, also known as GNE Myopathy or Nonaka Myopathy, is a rare genetic disorder that primarily affects the skeletal muscles. It is caused by mutations in the GNE gene, which plays a crucial role in the biosynthesis of sialic acid, a substance […]
In the rapidly advancing field of genetics, understanding the implications of specific gene mutations has become crucial for diagnosing and managing various conditions. Among these, the MYH2 gene plays a significant role, particularly in relation to Inclusion Body Myopathy. DNA Labs UAE, a leading genetic laboratory, offers a comprehensive genetic test specifically designed to analyze […]
Infantile Neuroaxonal Dystrophy (INAD) Type 1 is a rare genetic disorder that affects the nervous system. It is caused by mutations in the PLA2G6 gene, which plays a crucial role in the maintenance of neuronal health. This condition is characterized by a progressive decline in motor and cognitive functions, leading to severe neurological impairment. The […]
In the vast and intricate world of genetics, certain conditions remain rare yet profoundly impactful on the lives they touch. One such condition is SCN9A gene insensitivity to pain channelopathy. This condition, often shrouded in mystery, affects individuals in a way that most would find hard to imagine: they feel no pain. While at first, […]
Intellectual disability is a condition characterized by significant limitations in both intellectual functioning and in adaptive behavior, which covers many everyday social and practical skills. This condition manifests before the age of 18. Among the myriad causes of intellectual disabilities, genetic factors play a crucial role. One such genetic factor is mutations or alterations in […]
Intellectual disability (ID) is a broad term used to describe a range of cognitive and developmental impairments that manifest in childhood. It encompasses various conditions that affect mental capacity and adaptive behavior, making daily living skills challenging for those affected. Among the genetic causes of nonsyndromic intellectual disability, mutations in the CNKSR2 gene have been […]
Hydrocephalus is a condition characterized by an abnormal accumulation of cerebrospinal fluid (CSF) within the ventricles, or cavities, of the brain. This can lead to increased intracranial pressure inside the skull, potentially causing progressive enlargement of the head, convulsions, and mental disability. Hydrocephalus can be congenital or acquired, with various genetic factors playing a crucial […]
Intellectual disability (ID) is a broad term used to describe a range of cognitive and developmental impairments that affect an individual’s ability to learn, communicate, and live independently. One of the genetic factors contributing to intellectual disability is mutations in the TBR1 gene. DNA Labs UAE offers a comprehensive genetic test specifically designed to identify […]
— Hydrocephalus is a complex condition characterized by the abnormal accumulation of cerebrospinal fluid (CSF) within the ventricles of the brain. This accumulation can lead to increased intracranial pressure, which can cause a variety of neurological symptoms and, if left untreated, can be life-threatening. One specific type, known as MPDZ Gene Hydrocephalus Nonsyndromic Autosomal Recessive […]
Intestinal pseudo-obstruction is a condition that presents with symptoms similar to those of a blockage of the intestines but without any physical obstruction. It can be a challenging condition to diagnose due to the variety of its potential causes, including neurological, muscular, and genetic factors. Among the genetic causes, mutations in the FLNA gene have […]
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.
