Wolcott-Rallison Syndrome (WRS) is a rare genetic disorder primarily characterized by the onset of early infancy diabetes, multiple epiphyseal dysplasia, and a range of other possible systemic manifestations. The disorder is attributed to mutations in the EIF2AK3 gene, which plays a critical role in protein synthesis and the stress response of the endoplasmic reticulum. Due […]
Understanding the nuances of our genetic makeup has become a cornerstone of modern medicine, enabling us to predict, diagnose, and treat various genetic disorders with unprecedented precision. One such condition that has garnered attention is thyroid dyshormonogenesis type 1, a disorder stemming from mutations in the SLC5A5 gene. DNA Labs UAE stands at the forefront […]
In the quest to understand and manage thyroid disorders more effectively, genetic testing has emerged as a vital tool. Among the various genetic tests available, the TPO Gene Thyroid Dyshormonogenesis Type 2A Genetic Test stands out for its specificity in diagnosing a rare but significant condition affecting the thyroid gland. This article aims to shed […]
In the realm of genetic diagnostics and personalized medicine, understanding the nuances of specific genetic conditions is crucial for effective management and treatment. Thyroid dyshormonogenesis type 3, associated with mutations in the TG gene, is one such condition that underscores the importance of targeted genetic testing. DNA Labs UAE, a leading provider of genetic testing […]
Thyroid dyshormonogenesis is a condition that affects the thyroid gland’s ability to produce hormones properly. Among the various types, Type 4 is particularly noteworthy due to its genetic basis, involving mutations in the IYD gene. This condition can lead to significant health issues, including hypothyroidism, which necessitates an understanding of the symptoms and the availability […]
Renal tubular acidosis (RTA) is a medical condition characterized by the failure of the kidneys to properly acidify the urine. Among the various types of RTA, distal renal tubular acidosis (dRTA) is a significant form that is often inherited in an autosomal recessive manner. The ATP6V0A4 gene has been identified as one of the genetic […]
In the quest to understand and diagnose genetic disorders with precision, DNA Labs UAE stands at the forefront, offering a comprehensive range of genetic testing services. Among these, the SLC4A4 gene renal tubular acidosis proximal with ocular abnormalities genetic test is pivotal for diagnosing a rare but significant disorder. This test, priced at 4400 AED, […]
Renal tubular acidosis (RTA) is a medical condition that occurs when the kidneys fail to properly acidify the urine. This failure leads to the blood remaining too acidic, which can cause a host of complications throughout the body. One specific type of RTA, known as type 2 RTA or proximal RTA, can be related to […]
DNA Labs UAE is at the forefront of genetic testing and diagnostics, offering a wide range of services designed to provide insights into various genetic conditions. One such test is the ACE Gene Renal Tubular Dysgenesis Genetic Test. This detailed examination is specifically designed to detect mutations in the ACE gene, which can lead to […]
Renal Tubular Dysgenesis (RTD) is a rare, autosomal recessive disorder that primarily affects the kidneys. It is characterized by a lack of development (dysgenesis) of the kidney’s proximal tubules, leading to oligohydramnios (low amniotic fluid), which can result in fetal growth restriction and a spectrum of severe clinical manifestations post-birth. The AGT gene plays a […]
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.
