Cerebrotendinous Xanthomatosis (CTX) is a rare, inherited lipid storage disease caused by mutations in the CYP27A1 gene. This condition leads to abnormal storage of cholesterol and cholestanol in various tissues of the body, including the nervous system and tendons. Early diagnosis and treatment are crucial in managing the symptoms and preventing severe complications. DNA Labs […]
Cerebral Palsy (CP) is a group of permanent movement disorders that appear in early childhood. Spastic quadriplegia is the most severe form of cerebral palsy and involves all four limbs. The KANK1 gene has been identified as one of the genetic factors contributing to the development of Type 2 Spastic Quadriplegic Cerebral Palsy. Recognizing the […]
Cerebral palsy refers to a group of neurological disorders that appear in infancy or early childhood and permanently affect body movement and muscle coordination. Among the various types, Spastic Quadriplegia is one of the most severe forms, characterized by the stiffness of limbs on both sides of the body. Recent advancements in genetic research have […]
In the realm of medical science, understanding the genetic predispositions to certain conditions is a critical step in preventative healthcare. One such condition, cerebral infarction, commonly known as a stroke, has been linked to various genetic factors, including mutations in the PRKCH gene. DNA Labs UAE stands at the forefront of genetic testing, offering a […]
Cerebral Amyloid Angiopathy (CAA) is a neurological condition characterized by the accumulation of amyloid proteins in the walls of the arteries in the brain. This accumulation can lead to a variety of symptoms and is closely associated with the APP gene. DNA Labs UAE offers a comprehensive genetic test for those concerned about their risk […]
Cerebral Amyloid Angiopathy (CAA) is a neurological condition characterized by the accumulation of amyloid proteins in the walls of the arteries in the brain. This accumulation can lead to a range of symptoms and complications, including hemorrhagic stroke. One of the genes associated with an increased risk of developing CAA is the CST3 gene. Recognizing […]
DNA Labs UAE is at the forefront of genetic testing and diagnosis, offering a wide range of services designed to provide insights into various genetic conditions. Among these is the specialized genetic test for VLDLR Gene Cerebellar Hypoplasia and Mental Retardation with or without Quadrupedal Locomotion Type 1, a rare genetic disorder that affects brain […]
Cerebellar ataxia is a condition that affects the cerebellum, the part of the brain that controls muscle coordination. Among the various genetic mutations that can lead to cerebellar ataxia, mutations in the SNX14 gene are a notable cause. Recognizing the symptoms associated with SNX14 gene cerebellar ataxia and understanding the genetic testing options available are […]
In the realm of genetic testing and diagnosis, advancements have been pivotal in identifying and understanding various genetic disorders. One such condition that has garnered attention is the CAMTA1 gene cerebellar ataxia nonprogressive with mental retardation. This disorder, though rare, presents a unique set of challenges and symptoms for those affected. DNA Labs UAE stands […]
Understanding the complexities of genetic conditions is crucial for early diagnosis and management. Among these, the ATP8A2 gene-related disorders represent a significant concern due to their profound impact on individuals’ lives. Specifically, the condition known as Cerebellar Ataxia, Mental Retardation, and Dysequilibrium Syndrome Type 4 (CAMRQ4) has garnered attention within the medical community for its […]
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.
