Understanding the genetic makeup of individuals is crucial for diagnosing various inherited disorders. Among these, the Connexin 26 mutation holds significant importance due to its link with hearing loss and other health conditions. DNA Labs UAE is at the forefront of providing advanced genetic testing services, including the Connexin 26 Mutation Detection Test. This comprehensive […]
Symptoms of Myotonic Dystrophy Comprehensive Profile Test Myotonic dystrophy, a type of muscular dystrophy, is a genetic disorder that affects muscle function and other systems in the body. It is characterized by the inability of muscles to relax after contraction, which is known as myotonia. This condition can vary in severity and symptoms, often worsening […]
Spino-Bulbar Muscular Atrophy, also known as Kennedy’s disease, is a rare and inheritable neurological disorder that affects the nerve cells responsible for muscle movement. This condition leads to muscle weakness and atrophy, primarily affecting males, with symptoms usually appearing between the ages of 30 and 50. Early detection and understanding of the symptoms are crucial […]
Episodic Ataxia Type 1 (EA1) is a rare neurological disorder characterized by sudden, brief attacks of ataxia – a lack of muscle control or coordination of voluntary movements such as walking or picking up objects. These episodes can be accompanied by a range of other symptoms and are caused by mutations in the KCNA1 gene. […]
Symptoms of Episodic Ataxia Type 2 Hotspot Test Episodic ataxia type 2 (EA2) is a neurological condition characterized by sporadic bouts of ataxia, or lack of muscle coordination, often accompanied by vertigo, nausea, and headache. These episodes can last from minutes to days, significantly impacting the quality of life of those affected. Identifying the symptoms […]
Symptoms of NOTCH3 Mutation Detection CADASIL Test Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy, commonly known as CADASIL, is a genetic disorder that affects the small blood vessels in the brain. It is caused by mutations in the NOTCH3 gene, which plays a crucial role in the health and functioning of vascular smooth […]
In the realm of medical diagnostics, the advancement of specific antibody testing has been a cornerstone in the early detection and management of various neurological disorders. Among these, the Ganglioside GQ1b Antibody IgG Test stands out for its significance in diagnosing conditions associated with the peripheral nervous system. DNA Labs UAE is at the forefront […]
Symptoms of SCA Spinocerebellar Ataxia Comprehensive Profile Test Spinocerebellar Ataxia (SCA) is a term used for a group of hereditary ataxias that are characterized by degenerative changes in the part of the brain related to the movement control center, the cerebellum, and in some cases, the spinal cord. The complexity of SCA and its genetic […]
Episodic ataxia is a rare genetic condition characterized by sudden, temporary episodes of poor coordination and balance (ataxia). These episodes can be triggered by stress, physical exertion, or even sudden movements. Understanding and diagnosing episodic ataxia is crucial for managing its symptoms and improving the quality of life for those affected. DNA Labs UAE offers […]
MERRF syndrome, or Myoclonic Epilepsy with Ragged Red Fibers, is a rare, genetic disorder that primarily affects the nervous system and muscles. It is characterized by a variety of symptoms, which can vary significantly from person to person. Understanding these symptoms is crucial for early diagnosis and management of the condition. DNA Labs UAE offers […]
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.
