Neurology Diseases

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 […]

Hyperekplexia, also known as startle disease, is a rare genetic disorder characterized by an exaggerated startle reflex. This condition can lead to significant physical and psychological challenges for affected individuals. The GLRA1 gene plays a crucial role in the normal functioning of inhibitory glycine receptors in the brain. Mutations in the GLRA1 gene can disrupt […]

Understanding the symptoms of TIMM8A Gene Jensen Syndrome is crucial for early diagnosis and effective management of the condition. DNA Labs UAE offers a comprehensive genetic test specifically designed to identify mutations in the TIMM8A gene, which is associated with this rare genetic disorder. The cost of the test is 4400 AED, and it can […]

Hyperekplexia, also known as “startle disease,” is a rare, inherited neurological disorder characterized by an exaggerated startle response. This condition can be due to mutations in several genes, one of which is the GLRB gene. The GLRB gene provides instructions for making a component of glycine receptors in the brain. These receptors are critical for […]

Symptoms of INPP5E Gene Joubert Syndrome Type 1 Joubert Syndrome is a rare genetic disorder that affects the development of the cerebellum, a part of the brain that regulates motor skills, balance, and coordination. Among the various genetic mutations that can cause Joubert Syndrome, mutations in the INPP5E gene lead to a specific subtype known […]