Azoospermia, a condition characterized by the absence of sperm in the ejaculate, affects approximately 1% of the male population and is a significant cause of male infertility. Among the various factors contributing to azoospermia, Y chromosome microdeletions, specifically in the AZF (Azoospermia Factor) region, play a critical role. DNA Labs UAE offers a comprehensive genetic […]
Symptoms of CYP19A1 Gene Aromatase Deficiency Genetic Test Aromatase deficiency is a rare genetic condition caused by mutations in the CYP19A1 gene, which plays a crucial role in the synthesis of estrogen. Estrogen is a vital hormone in the development and functioning of both male and female reproductive systems, as well as in maintaining bone […]
Understanding the nuances of genetic conditions is crucial in the realm of medical science, particularly when it comes to conditions that affect sex development. One such condition that has garnered attention in recent years is the 46XY sex reversal, which is influenced by various genes, including the AKR1C4 gene. This condition can lead to discrepancies […]
— Understanding the Symptoms of SRY Gene 46XX Sex Reversal Type 1 Genetic Test The science of genetics has made significant strides in understanding the complexities of human development and the various factors that influence it. One area of interest is the study of sex determination and the conditions that lead to variations from typical […]
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 […]
Symptoms of LAS1L Gene Wilson-Turner Syndrome Genetic Test Wilson-Turner Syndrome is a rare genetic disorder that primarily affects males, characterized by intellectual disability, obesity, gynecomastia (enlarged breasts in males), and distinct facial features. It is caused by mutations in the LAS1L gene located on the X chromosome. Understanding the symptoms and undergoing genetic testing can […]
Symptoms of WT1 Gene Wilms Tumor Type 1 Familial Genetic Test Price 4400 AED Wilms tumor, also known as nephroblastoma, is a rare kidney cancer that primarily affects children. It is associated with mutations in the WT1 gene, which plays a crucial role in kidney development. Recognizing the symptoms early can lead to timely diagnosis […]
Vesicoureteral reflux (VUR) is a condition where urine flows backward from the bladder to the kidneys. This reverse flow can lead to various complications, including urinary tract infections and kidney damage. VUR is categorized into different types, with Type 3 being one of the classifications. Recent studies have identified a genetic link to VUR, specifically […]
Vesicoureteral reflux (VUR) is a condition where urine flows backward from the bladder to the kidneys. This reverse flow can lead to kidney infections and damage. There are various types of VUR, and one of the genetic forms is associated with mutations in the ROBO2 gene, known as Vesicoureteral reflux type 2. Understanding the symptoms […]
At DNA Labs UAE, we are dedicated to providing our clients with comprehensive genetic testing services that help in diagnosing and understanding various genetic disorders. One such condition that has come under increased scrutiny is the syndrome associated with mutations in the CRB2 gene, which can lead to ventriculomegaly and cystic kidney disease. This condition […]
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.
