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 […]
Reproductive Diseases
Symptoms and Testing information for FOXF2 Gene Disorders of sex development with cleft palate Genetic Test
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 […]
Symptoms and Testing information for CATSPER2 Gene Deafness and male infertility CATSPER2 related Genetic Test
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. […]
Symptoms and Testing information for STRC Gene Deafness and male infertility Genetic Test
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 […]
Symptoms and Testing information for RXFP2 Gene Cryptorchidism Genetic Test
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 […]
Symptoms and Testing information for CFTR Gene Congenital bilateral absence of vas deferens Genetic Test
Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) gene mutations can lead to a variety of health issues, one of which is the congenital bilateral absence of the vas deferens (CBAVD). This condition can significantly impact male fertility, making it crucial for those affected to understand the symptoms, implications, and available testing options. DNA Labs UAE offers […]
Symptoms and Testing information for AZF region Gene Azoospermia induced by Y chromosome microdeletions Genetic Test
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 and Testing information for CYP19A1 Gene Aromatase deficiency Genetic Test
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 […]
Symptoms and Testing information for AKR1C4 Gene 46XY sex reversal type 8 modifier of Genetic Test
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 […]
Symptoms and Testing information for MAMLD1 Gene Hypospadias type 2 X-linked Genetic Test
Hypospadias is a birth defect in males where the opening of the urethra is not located at the tip of the penis. Instead, it is found on the underside, which can vary from just below the tip to the base of the penile shaft, or even in the scrotum. This condition is one of the […]