The ZP1 gene plays a crucial role in the oocyte maturation process, which is essential for successful fertilization and subsequent embryo development. Mutations in the ZP1 gene can lead to oocyte maturation defects, potentially causing infertility in women. Understanding the symptoms associated with ZP1 gene mutations and the availability of genetic testing is crucial for […]
Symptoms of SOHLH1 Gene Oogenesis Dysfunction Genetic Test Oogenesis, the process by which the female gametes, or ova, are produced, is fundamental to fertility and reproductive health. A key gene implicated in this complex process is SOHLH1, which plays a crucial role in the early stages of oogenesis. Dysfunctions in the SOHLH1 gene can lead […]
Ovarian dysgenesis type 1 is a rare genetic condition that affects the normal development of the ovaries in females. It is primarily caused by mutations in the FSHR gene, which plays a critical role in the reproductive system. Understanding the symptoms of this condition is crucial for early diagnosis and management. DNA Labs UAE offers […]
Ovarian dysgenesis type 2, a rare genetic disorder, is primarily caused by mutations in the BMP15 gene. The BMP15 gene plays a crucial role in the development of female reproductive organs, particularly the ovaries. When mutations occur in this gene, it can lead to significant reproductive challenges, including infertility. Understanding the symptoms associated with this […]
Persistent Mullerian Duct Syndrome (PMDS) is a rare genetic condition that affects males. It is characterized by the presence of female reproductive structures such as a uterus and fallopian tubes, which normally should not be present in a male’s anatomy. This condition arises due to mutations in the AMH gene, leading to Type 1 PMDS. […]
Persistent Mullerian Duct Syndrome (PMDS) is a rare genetic condition that affects males. It is characterized by the persistence of female reproductive structures, such as the uterus and fallopian tubes, in a genetically male body. This condition is caused by mutations in the AMHR2 gene, which plays a crucial role in the regression of the […]
Preeclampsia is a complex condition that affects pregnant women, typically after the 20th week of pregnancy. It is characterized by high blood pressure and often a significant amount of protein in the urine. The CORIN gene plays a crucial role in the cardiovascular system, and mutations in this gene have been linked to an increased […]
Recurrent pregnancy loss (RPL) is a distressing condition that affects many couples worldwide, leading to significant emotional distress and uncertainty. Recent advancements in genetic research have identified various genetic factors that contribute to RPL, among which the C4BPA gene plays a significant role. DNA Labs UAE is at the forefront of providing comprehensive genetic testing, […]
In the realm of genetic testing and diagnostics, DNA Labs UAE stands at the forefront, offering a comprehensive suite of tests designed to unveil intricate genetic conditions. Among these, the HSD17B3 Gene Pseudohermaphroditism with Gynecomastia Genetic Test is pivotal for individuals experiencing symptoms aligned with this rare genetic condition. This test, priced at 4400 AED, […]
Symptoms of NSMF Gene Hypogonadotropic Hypogonadism Genetic Test Hypogonadotropic hypogonadism (HH) is a condition characterized by the inadequate secretion of sex hormones due to the malfunctioning of the gonadotropin-releasing hormone (GnRH) in the hypothalamus or the pituitary gland’s response to GnRH. When this condition is linked to mutations in the NSMF gene, it is essential […]
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.
