Symptoms of LHCGR Gene Leydig Cell Hypoplasia Type 1 Genetic Test Leydig cell hypoplasia (LCH) is a rare disorder of sex development (DSD), specifically affecting the production of male sex hormones due to mutations in the LHCGR gene. This condition is characterized by a spectrum of symptoms that can vary significantly among affected individuals. Recognizing […]
Cryptorchidism is a condition that affects newborn boys, characterized by the failure of one or both testes to descend into the scrotum. While the exact cause of cryptorchidism can be multifactorial, involving both genetic and environmental factors, recent research has highlighted the significance of the RXFP2 gene in its development. DNA Labs UAE is at […]
In the realm of genetic testing, advancements have made it possible to identify and understand the genetic underpinnings of many conditions that affect humans. Among these, the STRC gene has been identified as a significant marker for certain types of deafness and has also been implicated in male infertility. DNA Labs UAE, a leading genetic […]
The CATSPER2 gene plays a pivotal role in human physiology, influencing both auditory function and male fertility. Mutations in the CATSPER2 gene can lead to a unique combination of symptoms, primarily characterized by deafness and male infertility. Understanding these symptoms and the available genetic testing options is crucial for individuals who may be at risk. […]
DNA Labs UAE stands at the forefront of genetic testing, offering a wide range of services aimed at providing individuals with the information they need to make informed health and lifestyle decisions. One of the specialized tests offered is focused on the FOXF2 gene, known to be associated with disorders of sex development (DSD) and […]
The FSHB gene plays a critical role in the reproductive system of both males and females. It encodes for the beta subunit of the follicle-stimulating hormone (FSH), which is essential for the growth and maturation of ovarian follicles in females and spermatogenesis in males. A deficiency in the FSH hormone due to mutations in the […]
Guttmacher syndrome, also known as hand-foot-genital syndrome, is a rare genetic condition that affects the development of the hands, feet, and genitourinary system. This condition is caused by mutations in the HOXA13 gene, which plays a critical role in the embryonic development of these structures. Understanding the symptoms of Guttmacher syndrome is crucial for early […]
Hand-foot-uterus syndrome, also known as hand-foot-genital syndrome, is a rare genetic condition that affects the development of the hands, feet, and urogenital system. This condition is caused by mutations in the HOXA13 gene, which plays a crucial role in the embryonic development of these structures. Understanding the symptoms and seeking timely genetic testing can be […]
In the quest to understand the complexities of human genetics and its implications on health, DNA Labs UAE stands at the forefront, offering a range of genetic testing services designed to provide insights into various genetic conditions. Among these, the NLRP7 Gene Hydatidiform Mole Genetic Test is particularly significant for its role in diagnosing a […]
Hydatidiform mole, also known as a molar pregnancy, is a rare condition that occurs during pregnancy. The condition is characterized by the abnormal growth of trophoblasts, the cells that normally develop into the placenta. There are two types of hydatidiform moles: complete and partial. In some cases, women may experience recurrent hydatidiform moles, a 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.
