Symptoms of ST3GAL5 Gene Amish Infantile Epilepsy Syndrome Amish Infantile Epilepsy Syndrome, also known as ST3GAL5 deficiency, is a rare genetic disorder that predominantly affects the Amish community. This condition is characterized by a spectrum of neurological symptoms, primarily due to mutations in the ST3GAL5 gene. Understanding the symptoms associated with this syndrome is crucial […]
— TTR Gene Amyloidosis is a progressively debilitating condition that affects various organs and tissues in the body. This genetic disorder is caused by mutations in the transthyretin (TTR) gene, which leads to the abnormal accumulation of amyloid proteins in the body’s organs and tissues, impairing their normal function. Recognizing the symptoms early is crucial […]
DNA Labs UAE is at the forefront of genetic testing, offering a comprehensive suite of tests designed to identify a range of genetic conditions. Among these, the DCPS Gene Al-Raqad Syndrome Genetic Test is pivotal for diagnosing the rare and complex Al-Raqad syndrome. This article delves into the symptoms associated with Al-Raqad syndrome, the significance […]
Symptoms of GFAP Gene Alexander Disease Genetic Test Alexander disease is a rare and often fatal neurological disorder, which is one of a group of neurological conditions known as the leukodystrophies. These disorders affect the growth or maintenance of the myelin sheath, which is the fatty covering that insulates nerve fibers. Alexander disease is specifically […]
Understanding the complexities of genetic disorders is pivotal in today’s healthcare landscape. Among these, the AAAS Gene Achalasia Addisonianism Alacrimia Syndrome, commonly abbreviated as Triple A Syndrome, stands out due to its rarity and the intricacies involved in its diagnosis and management. DNA Labs UAE, a leading institution in genetic testing, offers comprehensive insights and […]
In the realm of genetic testing, advancements have paved the way for early detection and management of various inherited disorders. One such condition that has garnered attention is Allan-Herndon-Dudley Syndrome (AHDS), a rare X-linked recessive disorder. AHDS is caused by mutations in the SLC16A2 gene, which plays a critical role in the development and function […]
Acrocallosal Syndrome (ACS) is a rare genetic disorder that presents with a range of physical and cognitive symptoms due to abnormalities in the KIF7 gene. Understanding this condition, its symptoms, and the genetic testing available is crucial for families and individuals who may be affected. DNA Labs UAE is at the forefront of providing comprehensive […]
The ATRX Gene Alpha-thalassemia/mental retardation syndrome (ATR-X) is a rare and complex genetic condition that affects various aspects of physical and intellectual development. This condition, primarily found in males, is characterized by a combination of alpha-thalassemia, a blood disorder that reduces the production of hemoglobin, and mental retardation, along with a variety of other possible […]
Understanding genetic disorders and their implications is essential for managing health and preventing severe complications. One such genetic condition is the deficiency of the ACOX1 gene, which leads to acyl-CoA oxidase deficiency. This disorder affects the body’s ability to break down certain fats, leading to an accumulation that can cause damage to organs and tissues. […]
Alternating Hemiplegia of Childhood (AHC) is a rare neurological disorder that typically manifests in infancy or early childhood. It is characterized by recurrent episodes of paralysis on one side of the body (hemiplegia), which can switch sides. These episodes can last from minutes to days. The ATP1A2 gene has been identified as one of the […]
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.
