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 […]
Reproductive Diseases
Symptoms and Testing information for FSHB Gene Follicle-stimulating hormone deficiency isolated Genetic Test
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 […]
Symptoms and Testing information for HOXA13 Gene Guttmacher syndrome Genetic Test
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 […]
Symptoms and Testing information for HOXA13 Gene Hand-foot-uterus syndrome Genetic Test
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 […]
Symptoms and Testing information for NLRP7 Gene Hydatidiform mole Genetic Test
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 […]
Symptoms and Testing information for KHDC3L Gene Hydatidiform mole recurrent type 2 Genetic Test
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 […]
Symptoms and Testing information for KISS1 Gene Hypogonadotropic hypogonadism Genetic Test
Understanding the complexities of our genetic makeup can unlock answers to numerous health conditions that were once shrouded in mystery. One such condition is Hypogonadotropic Hypogonadism (HH), a disorder characterized by the inadequate secretion of gonadotropin-releasing hormone by the hypothalamus, which affects the development and function of the gonads (ovaries or testes). This can lead […]
Symptoms and Testing information for NSMF Gene Hypogonadotropic hypogonadism Genetic Test
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 […]
Symptoms and Testing information for FGF8 Gene Hypogonadotropic hypogonadism type 6 with or without anosmia Genetic Test
Symptoms of FGF8 Gene Hypogonadotropic Hypogonadism Type 6 with or Without Anosmia Genetic Test Hypogonadotropic hypogonadism type 6, caused by mutations in the FGF8 gene, is a condition that affects the development and function of the gonads, leading to reduced or absent production of sex hormones and, consequently, delayed or absent puberty. This condition can […]
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 […]